Canonical Allele Identifier: CA367889290

Gene: ELN

Linked Data

• MyVariant Identifiers: chr7:g.73477491G>A (hg19) ; chr7:g.74063161G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74063161G>A , CM000669.2:g.74063161G>A	GRCh38
NC_000007.13:g.73477491G>A , CM000669.1:g.73477491G>A	GRCh37
NC_000007.12:g.73115427G>A	NCBI36
NG_009261.1:g.40065G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000692049.1:c.1981G>A	ENSP00000510104.1:p.Val661Met
ENST00000252034.12:c.1795G>A MANE Select	ENSP00000252034.7:p.Val599Met
ENST00000252034.11:c.1795G>A	ENSP00000252034.7:p.Val599Met
ENST00000320399.10:c.1894G>A	ENSP00000313565.6:p.Val632Met
ENST00000320492.11:c.1552G>A	ENSP00000315607.7:p.Val518Met
ENST00000357036.9:c.1810G>A	ENSP00000349540.5:p.Val604Met
ENST00000358929.8:c.1981G>A	ENSP00000351807.5:p.Val661Met
ENST00000380553.8:c.1387G>A	ENSP00000369926.4:p.Val463Met
ENST00000380562.8:c.1813G>A	ENSP00000369936.4:p.Val605Met
ENST00000380575.8:c.1708G>A	ENSP00000369949.4:p.Val570Met
ENST00000380576.9:c.1738G>A	ENSP00000369950.5:p.Val580Met
ENST00000380584.8:c.1651G>A	ENSP00000369958.4:p.Val551Met
ENST00000414324.5:c.1723G>A	ENSP00000392575.1:p.Val575Met
ENST00000429192.5:c.1753G>A	ENSP00000391129.1:p.Val585Met
ENST00000445912.5:c.1795G>A	ENSP00000389857.1:p.Val599Met
ENST00000458204.5:c.1765G>A	ENSP00000403162.1:p.Val589Met
ENST00000621115.4:c.1528G>A	ENSP00000480955.1:p.Val510Met
NM_000501.3:c.1795G>A	NP_000492.2:p.Val599Met
NM_001081752.2:c.1708G>A	NP_001075221.1:p.Val570Met
NM_001081753.2:c.1753G>A	NP_001075222.1:p.Val585Met
NM_001081754.2:c.1810G>A	NP_001075223.1:p.Val604Met
NM_001081755.2:c.1738G>A	NP_001075224.1:p.Val580Met
NM_001278912.1:c.1795G>A	NP_001265841.1:p.Val599Met
NM_001278913.1:c.1552G>A	NP_001265842.1:p.Val518Met
NM_001278914.1:c.1723G>A	NP_001265843.1:p.Val575Met
NM_001278915.1:c.1813G>A	NP_001265844.1:p.Val605Met
NM_001278916.1:c.1651G>A	NP_001265845.1:p.Val551Met
NM_001278917.1:c.1765G>A	NP_001265846.1:p.Val589Met
NM_001278918.1:c.1528G>A	NP_001265847.1:p.Val510Met
NM_001278939.1:c.1981G>A	NP_001265868.1:p.Val661Met
XM_005250187.1:c.1759G>A	XP_005250244.1:p.Val587Met
XM_005250188.1:c.1753G>A	XP_005250245.1:p.Val585Met
XM_011515868.1:c.1810G>A	XP_011514170.1:p.Val604Met
XM_011515869.1:c.1780G>A	XP_011514171.1:p.Val594Met
XM_011515870.1:c.1774G>A	XP_011514172.1:p.Val592Met
XM_011515871.1:c.1768G>A	XP_011514173.1:p.Val590Met
XM_011515872.1:c.1756G>A	XP_011514174.1:p.Val586Met
XM_011515873.1:c.1753G>A	XP_011514175.1:p.Val585Met
XM_011515874.1:c.1744G>A	XP_011514176.1:p.Val582Met
XM_011515875.1:c.1729G>A	XP_011514177.1:p.Val577Met
XM_011515876.1:c.1810G>A	XP_011514178.1:p.Val604Met
XM_011515877.1:c.1699G>A	XP_011514179.1:p.Val567Met
XM_005250187.2:c.1759G>A	XP_005250244.1:p.Val587Met
XM_005250188.2:c.1753G>A	XP_005250245.1:p.Val585Met
XM_011515868.2:c.1810G>A	XP_011514170.1:p.Val604Met
XM_011515871.2:c.1768G>A	XP_011514173.1:p.Val590Met
XM_011515872.2:c.1756G>A	XP_011514174.1:p.Val586Met
XM_011515873.2:c.1753G>A	XP_011514175.1:p.Val585Met
XM_011515875.2:c.1729G>A	XP_011514177.1:p.Val577Met
XM_011515876.2:c.1810G>A	XP_011514178.1:p.Val604Met
XM_011515877.2:c.1699G>A	XP_011514179.1:p.Val567Met
XM_017011813.1:c.1723G>A	XP_016867302.1:p.Val575Met
XM_017011814.2:c.1711G>A	XP_016867303.1:p.Val571Met
NM_000501.4:c.1795G>A MANE Select	NP_000492.2:p.Val599Met
NM_001081752.3:c.1708G>A	NP_001075221.1:p.Val570Met
NM_001081753.3:c.1753G>A	NP_001075222.1:p.Val585Met
NM_001081754.3:c.1810G>A	NP_001075223.1:p.Val604Met
NM_001081755.3:c.1738G>A	NP_001075224.1:p.Val580Met
NM_001278912.2:c.1795G>A	NP_001265841.1:p.Val599Met
NM_001278913.2:c.1552G>A	NP_001265842.1:p.Val518Met
NM_001278914.2:c.1723G>A	NP_001265843.1:p.Val575Met
NM_001278915.2:c.1813G>A	NP_001265844.1:p.Val605Met
NM_001278916.2:c.1651G>A	NP_001265845.1:p.Val551Met
NM_001278917.2:c.1765G>A	NP_001265846.1:p.Val589Met
NM_001278918.2:c.1528G>A	NP_001265847.1:p.Val510Met
NM_001278939.2:c.1981G>A	NP_001265868.1:p.Val661Met