Canonical Allele Identifier: CA281482

Gene: ELN

Linked Data

• ClinVar Variation Id: 163398
• ClinVar RCV Id: RCV000150646
• dbSNP Id: rs727503035
• MyVariant Identifiers: chr7:g.73477700G>A (hg19) ; chr7:g.74063370G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74063370G>A , CM000669.2:g.74063370G>A	GRCh38
NC_000007.13:g.73477700G>A , CM000669.1:g.73477700G>A	GRCh37
NC_000007.12:g.73115636G>A	NCBI36
NG_009261.1:g.40274G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000692049.1:c.2104+1G>A	ENSP00000510104.1:n.2104+1G>A
ENST00000252034.12:c.1918+1G>A MANE Select	ENSP00000252034.7:n.1918+1G>A
ENST00000252034.11:c.1918+1G>A	ENSP00000252034.7:n.1918+1G>A
ENST00000320399.10:c.2017+1G>A	ENSP00000313565.6:n.2017+1G>A
ENST00000320492.11:c.1675+1G>A	ENSP00000315607.7:n.1675+1G>A
ENST00000357036.9:c.1933+1G>A	ENSP00000349540.5:n.1933+1G>A
ENST00000358929.8:c.2104+1G>A	ENSP00000351807.5:n.2104+1G>A
ENST00000380553.8:c.1510+1G>A	ENSP00000369926.4:n.1510+1G>A
ENST00000380562.8:c.1936+1G>A	ENSP00000369936.4:n.1936+1G>A
ENST00000380575.8:c.1831+1G>A	ENSP00000369949.4:n.1831+1G>A
ENST00000380576.9:c.1861+1G>A	ENSP00000369950.5:n.1861+1G>A
ENST00000380584.8:c.1774+1G>A	ENSP00000369958.4:n.1774+1G>A
ENST00000414324.5:c.1846+1G>A	ENSP00000392575.1:n.1846+1G>A
ENST00000429192.5:c.1876+1G>A	ENSP00000391129.1:n.1876+1G>A
ENST00000445912.5:c.1918+1G>A	ENSP00000389857.1:n.1918+1G>A
ENST00000458204.5:c.1888+1G>A	ENSP00000403162.1:n.1888+1G>A
ENST00000621115.4:c.1651+1G>A	ENSP00000480955.1:n.1651+1G>A
NM_000501.3:c.1918+1G>A	NP_000492.2:n.1918+1G>A
NM_001081752.2:c.1831+1G>A	NP_001075221.1:n.1831+1G>A
NM_001081753.2:c.1876+1G>A	NP_001075222.1:n.1876+1G>A
NM_001081754.2:c.1933+1G>A	NP_001075223.1:n.1933+1G>A
NM_001081755.2:c.1861+1G>A	NP_001075224.1:n.1861+1G>A
NM_001278912.1:c.1918+1G>A	NP_001265841.1:n.1918+1G>A
NM_001278913.1:c.1675+1G>A	NP_001265842.1:n.1675+1G>A
NM_001278914.1:c.1846+1G>A	NP_001265843.1:n.1846+1G>A
NM_001278915.1:c.1936+1G>A	NP_001265844.1:n.1936+1G>A
NM_001278916.1:c.1774+1G>A	NP_001265845.1:n.1774+1G>A
NM_001278917.1:c.1888+1G>A	NP_001265846.1:n.1888+1G>A
NM_001278918.1:c.1651+1G>A	NP_001265847.1:n.1651+1G>A
NM_001278939.1:c.2104+1G>A	NP_001265868.1:n.2104+1G>A
XM_005250187.1:c.1882+1G>A	XP_005250244.1:n.1882+1G>A
XM_005250188.1:c.1876+1G>A	XP_005250245.1:n.1876+1G>A
XM_011515868.1:c.1933+1G>A	XP_011514170.1:n.1933+1G>A
XM_011515869.1:c.1903+1G>A	XP_011514171.1:n.1903+1G>A
XM_011515870.1:c.1897+1G>A	XP_011514172.1:n.1897+1G>A
XM_011515871.1:c.1891+1G>A	XP_011514173.1:n.1891+1G>A
XM_011515872.1:c.1879+1G>A	XP_011514174.1:n.1879+1G>A
XM_011515873.1:c.1876+1G>A	XP_011514175.1:n.1876+1G>A
XM_011515874.1:c.1867+1G>A	XP_011514176.1:n.1867+1G>A
XM_011515875.1:c.1852+1G>A	XP_011514177.1:n.1852+1G>A
XM_011515876.1:c.1933+1G>A	XP_011514178.1:n.1933+1G>A
XM_011515877.1:c.1822+1G>A	XP_011514179.1:n.1822+1G>A
XM_005250187.2:c.1882+1G>A	XP_005250244.1:n.1882+1G>A
XM_005250188.2:c.1876+1G>A	XP_005250245.1:n.1876+1G>A
XM_011515868.2:c.1933+1G>A	XP_011514170.1:n.1933+1G>A
XM_011515871.2:c.1891+1G>A	XP_011514173.1:n.1891+1G>A
XM_011515872.2:c.1879+1G>A	XP_011514174.1:n.1879+1G>A
XM_011515873.2:c.1876+1G>A	XP_011514175.1:n.1876+1G>A
XM_011515875.2:c.1852+1G>A	XP_011514177.1:n.1852+1G>A
XM_011515876.2:c.1933+1G>A	XP_011514178.1:n.1933+1G>A
XM_011515877.2:c.1822+1G>A	XP_011514179.1:n.1822+1G>A
XM_017011813.1:c.1846+1G>A	XP_016867302.1:n.1846+1G>A
XM_017011814.2:c.1834+1G>A	XP_016867303.1:n.1834+1G>A
NM_000501.4:c.1918+1G>A MANE Select	NP_000492.2:n.1918+1G>A
NM_001081752.3:c.1831+1G>A	NP_001075221.1:n.1831+1G>A
NM_001081753.3:c.1876+1G>A	NP_001075222.1:n.1876+1G>A
NM_001081754.3:c.1933+1G>A	NP_001075223.1:n.1933+1G>A
NM_001081755.3:c.1861+1G>A	NP_001075224.1:n.1861+1G>A
NM_001278912.2:c.1918+1G>A	NP_001265841.1:n.1918+1G>A
NM_001278913.2:c.1675+1G>A	NP_001265842.1:n.1675+1G>A
NM_001278914.2:c.1846+1G>A	NP_001265843.1:n.1846+1G>A
NM_001278915.2:c.1936+1G>A	NP_001265844.1:n.1936+1G>A
NM_001278916.2:c.1774+1G>A	NP_001265845.1:n.1774+1G>A
NM_001278917.2:c.1888+1G>A	NP_001265846.1:n.1888+1G>A
NM_001278918.2:c.1651+1G>A	NP_001265847.1:n.1651+1G>A
NM_001278939.2:c.2104+1G>A	NP_001265868.1:n.2104+1G>A