Canonical Allele Identifier: CA455883856

Gene: ELN

Linked Data

• gnomAD v4: 7-74054738-T-A
• MyVariant Identifiers: chr7:g.73469068T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74054738T>A , CM000669.2:g.74054738T>A	GRCh38
NC_000007.13:g.73469068T>A , CM000669.1:g.73469068T>A	GRCh37
NC_000007.12:g.73107004T>A	NCBI36
NG_009261.1:g.31642T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000692049.1:c.1119T>A	ENSP00000510104.1:p.Ala373=
ENST00000252034.12:c.1119T>A MANE Select	ENSP00000252034.7:p.Ala373=
ENST00000252034.11:c.1119T>A	ENSP00000252034.7:p.Ala373=
ENST00000320399.10:c.1119T>A	ENSP00000313565.6:p.Ala373=
ENST00000320492.11:c.1011T>A	ENSP00000315607.7:p.Ala337=
ENST00000357036.9:c.1134T>A	ENSP00000349540.5:p.Ala378=
ENST00000358929.8:c.1119T>A	ENSP00000351807.5:p.Ala373=
ENST00000380553.8:c.768T>A	ENSP00000369926.4:p.Ala256=
ENST00000380562.8:c.1119T>A	ENSP00000369936.4:p.Ala373=
ENST00000380575.8:c.1089T>A	ENSP00000369949.4:p.Ala363=
ENST00000380576.9:c.1119T>A	ENSP00000369950.5:p.Ala373=
ENST00000380584.8:c.1077T>A	ENSP00000369958.4:p.Ala359=
ENST00000414324.5:c.1104T>A	ENSP00000392575.1:p.Ala368=
ENST00000429192.5:c.1134T>A	ENSP00000391129.1:p.Ala378=
ENST00000445912.5:c.1119T>A	ENSP00000389857.1:p.Ala373=
ENST00000458204.5:c.1089T>A	ENSP00000403162.1:p.Ala363=
ENST00000466878.5:n.438T>A
ENST00000492210.1:n.482T>A
ENST00000621115.4:c.987T>A	ENSP00000480955.1:p.Ala329=
NM_000501.3:c.1119T>A	NP_000492.2:p.Ala373=
NM_001081752.2:c.1089T>A	NP_001075221.1:p.Ala363=
NM_001081753.2:c.1134T>A	NP_001075222.1:p.Ala378=
NM_001081754.2:c.1134T>A	NP_001075223.1:p.Ala378=
NM_001081755.2:c.1119T>A	NP_001075224.1:p.Ala373=
NM_001278912.1:c.1119T>A	NP_001265841.1:p.Ala373=
NM_001278913.1:c.1011T>A	NP_001265842.1:p.Ala337=
NM_001278914.1:c.1104T>A	NP_001265843.1:p.Ala368=
NM_001278915.1:c.1119T>A	NP_001265844.1:p.Ala373=
NM_001278916.1:c.1077T>A	NP_001265845.1:p.Ala359=
NM_001278917.1:c.1089T>A	NP_001265846.1:p.Ala363=
NM_001278918.1:c.987T>A	NP_001265847.1:p.Ala329=
NM_001278939.1:c.1119T>A	NP_001265868.1:p.Ala373=
XM_005250187.1:c.1083T>A	XP_005250244.1:p.Ala361=
XM_005250188.1:c.1077T>A	XP_005250245.1:p.Ala359=
XM_011515868.1:c.1134T>A	XP_011514170.1:p.Ala378=
XM_011515869.1:c.1104T>A	XP_011514171.1:p.Ala368=
XM_011515870.1:c.1098T>A	XP_011514172.1:p.Ala366=
XM_011515871.1:c.1092T>A	XP_011514173.1:p.Ala364=
XM_011515872.1:c.1111+1429T>A	XP_011514174.1:n.1111+1429T>A
XM_011515873.1:c.1134T>A	XP_011514175.1:p.Ala378=
XM_011515874.1:c.1068T>A	XP_011514176.1:p.Ala356=
XM_011515875.1:c.1053T>A	XP_011514177.1:p.Ala351=
XM_011515876.1:c.1134T>A	XP_011514178.1:p.Ala378=
XM_011515877.1:c.1111+1429T>A	XP_011514179.1:n.1111+1429T>A
XM_005250187.2:c.1083T>A	XP_005250244.1:p.Ala361=
XM_005250188.2:c.1077T>A	XP_005250245.1:p.Ala359=
XM_011515868.2:c.1134T>A	XP_011514170.1:p.Ala378=
XM_011515871.2:c.1092T>A	XP_011514173.1:p.Ala364=
XM_011515872.2:c.1111+1429T>A	XP_011514174.1:n.1111+1429T>A
XM_011515873.2:c.1134T>A	XP_011514175.1:p.Ala378=
XM_011515875.2:c.1053T>A	XP_011514177.1:p.Ala351=
XM_011515876.2:c.1134T>A	XP_011514178.1:p.Ala378=
XM_011515877.2:c.1111+1429T>A	XP_011514179.1:n.1111+1429T>A
XM_017011813.1:c.1047T>A	XP_016867302.1:p.Ala349=
XM_017011814.2:c.1092T>A	XP_016867303.1:p.Ala364=
NM_000501.4:c.1119T>A MANE Select	NP_000492.2:p.Ala373=
NM_001081752.3:c.1089T>A	NP_001075221.1:p.Ala363=
NM_001081753.3:c.1134T>A	NP_001075222.1:p.Ala378=
NM_001081754.3:c.1134T>A	NP_001075223.1:p.Ala378=
NM_001081755.3:c.1119T>A	NP_001075224.1:p.Ala373=
NM_001278912.2:c.1119T>A	NP_001265841.1:p.Ala373=
NM_001278913.2:c.1011T>A	NP_001265842.1:p.Ala337=
NM_001278914.2:c.1104T>A	NP_001265843.1:p.Ala368=
NM_001278915.2:c.1119T>A	NP_001265844.1:p.Ala373=
NM_001278916.2:c.1077T>A	NP_001265845.1:p.Ala359=
NM_001278917.2:c.1089T>A	NP_001265846.1:p.Ala363=
NM_001278918.2:c.987T>A	NP_001265847.1:p.Ala329=
NM_001278939.2:c.1119T>A	NP_001265868.1:p.Ala373=