Canonical Allele Identifier: CA455886904

Gene: ELN

Linked Data

• MyVariant Identifiers: chr7:g.73477520T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74063190T>C , CM000669.2:g.74063190T>C	GRCh38
NC_000007.13:g.73477520T>C , CM000669.1:g.73477520T>C	GRCh37
NC_000007.12:g.73115456T>C	NCBI36
NG_009261.1:g.40094T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000692049.1:c.2010T>C	ENSP00000510104.1:p.Ala670=
ENST00000252034.12:c.1824T>C MANE Select	ENSP00000252034.7:p.Ala608=
ENST00000252034.11:c.1824T>C	ENSP00000252034.7:p.Ala608=
ENST00000320399.10:c.1923T>C	ENSP00000313565.6:p.Ala641=
ENST00000320492.11:c.1581T>C	ENSP00000315607.7:p.Ala527=
ENST00000357036.9:c.1839T>C	ENSP00000349540.5:p.Ala613=
ENST00000358929.8:c.2010T>C	ENSP00000351807.5:p.Ala670=
ENST00000380553.8:c.1416T>C	ENSP00000369926.4:p.Ala472=
ENST00000380562.8:c.1842T>C	ENSP00000369936.4:p.Ala614=
ENST00000380575.8:c.1737T>C	ENSP00000369949.4:p.Ala579=
ENST00000380576.9:c.1767T>C	ENSP00000369950.5:p.Ala589=
ENST00000380584.8:c.1680T>C	ENSP00000369958.4:p.Ala560=
ENST00000414324.5:c.1752T>C	ENSP00000392575.1:p.Ala584=
ENST00000429192.5:c.1782T>C	ENSP00000391129.1:p.Ala594=
ENST00000445912.5:c.1824T>C	ENSP00000389857.1:p.Ala608=
ENST00000458204.5:c.1794T>C	ENSP00000403162.1:p.Ala598=
ENST00000621115.4:c.1557T>C	ENSP00000480955.1:p.Ala519=
NM_000501.3:c.1824T>C	NP_000492.2:p.Ala608=
NM_001081752.2:c.1737T>C	NP_001075221.1:p.Ala579=
NM_001081753.2:c.1782T>C	NP_001075222.1:p.Ala594=
NM_001081754.2:c.1839T>C	NP_001075223.1:p.Ala613=
NM_001081755.2:c.1767T>C	NP_001075224.1:p.Ala589=
NM_001278912.1:c.1824T>C	NP_001265841.1:p.Ala608=
NM_001278913.1:c.1581T>C	NP_001265842.1:p.Ala527=
NM_001278914.1:c.1752T>C	NP_001265843.1:p.Ala584=
NM_001278915.1:c.1842T>C	NP_001265844.1:p.Ala614=
NM_001278916.1:c.1680T>C	NP_001265845.1:p.Ala560=
NM_001278917.1:c.1794T>C	NP_001265846.1:p.Ala598=
NM_001278918.1:c.1557T>C	NP_001265847.1:p.Ala519=
NM_001278939.1:c.2010T>C	NP_001265868.1:p.Ala670=
XM_005250187.1:c.1788T>C	XP_005250244.1:p.Ala596=
XM_005250188.1:c.1782T>C	XP_005250245.1:p.Ala594=
XM_011515868.1:c.1839T>C	XP_011514170.1:p.Ala613=
XM_011515869.1:c.1809T>C	XP_011514171.1:p.Ala603=
XM_011515870.1:c.1803T>C	XP_011514172.1:p.Ala601=
XM_011515871.1:c.1797T>C	XP_011514173.1:p.Ala599=
XM_011515872.1:c.1785T>C	XP_011514174.1:p.Ala595=
XM_011515873.1:c.1782T>C	XP_011514175.1:p.Ala594=
XM_011515874.1:c.1773T>C	XP_011514176.1:p.Ala591=
XM_011515875.1:c.1758T>C	XP_011514177.1:p.Ala586=
XM_011515876.1:c.1839T>C	XP_011514178.1:p.Ala613=
XM_011515877.1:c.1728T>C	XP_011514179.1:p.Ala576=
XM_005250187.2:c.1788T>C	XP_005250244.1:p.Ala596=
XM_005250188.2:c.1782T>C	XP_005250245.1:p.Ala594=
XM_011515868.2:c.1839T>C	XP_011514170.1:p.Ala613=
XM_011515871.2:c.1797T>C	XP_011514173.1:p.Ala599=
XM_011515872.2:c.1785T>C	XP_011514174.1:p.Ala595=
XM_011515873.2:c.1782T>C	XP_011514175.1:p.Ala594=
XM_011515875.2:c.1758T>C	XP_011514177.1:p.Ala586=
XM_011515876.2:c.1839T>C	XP_011514178.1:p.Ala613=
XM_011515877.2:c.1728T>C	XP_011514179.1:p.Ala576=
XM_017011813.1:c.1752T>C	XP_016867302.1:p.Ala584=
XM_017011814.2:c.1740T>C	XP_016867303.1:p.Ala580=
NM_000501.4:c.1824T>C MANE Select	NP_000492.2:p.Ala608=
NM_001081752.3:c.1737T>C	NP_001075221.1:p.Ala579=
NM_001081753.3:c.1782T>C	NP_001075222.1:p.Ala594=
NM_001081754.3:c.1839T>C	NP_001075223.1:p.Ala613=
NM_001081755.3:c.1767T>C	NP_001075224.1:p.Ala589=
NM_001278912.2:c.1824T>C	NP_001265841.1:p.Ala608=
NM_001278913.2:c.1581T>C	NP_001265842.1:p.Ala527=
NM_001278914.2:c.1752T>C	NP_001265843.1:p.Ala584=
NM_001278915.2:c.1842T>C	NP_001265844.1:p.Ala614=
NM_001278916.2:c.1680T>C	NP_001265845.1:p.Ala560=
NM_001278917.2:c.1794T>C	NP_001265846.1:p.Ala598=
NM_001278918.2:c.1557T>C	NP_001265847.1:p.Ala519=
NM_001278939.2:c.2010T>C	NP_001265868.1:p.Ala670=