Canonical Allele Identifier: CA467474478

Gene: ENG

Linked Data

• gnomAD v4: 9-127815757-G-T
• MyVariant Identifiers: chr9:g.130578036G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127815757G>T , CM000671.2:g.127815757G>T	GRCh38
NC_000009.11:g.130578036G>T , CM000671.1:g.130578036G>T	GRCh37
NC_000009.10:g.129617857G>T	NCBI36
NG_009551.1:g.44012C>A , LRG_589:g.44012C>A
NG_023245.1:g.17883G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.1356C>A	ENSP00000479015.1:p.Ser452=
ENST00000373203.9:c.1902C>A MANE Select	ENSP00000362299.4:p.Ser634=
ENST00000344849.4:c.*160C>A	ENSP00000341917.3:n.*160C>A
ENST00000373203.8:c.1902C>A	ENSP00000362299.4:p.Ser634=
ENST00000480266.5:c.1356C>A	ENSP00000479015.1:p.Ser452=
NM_000118.3:c.*160C>A , LRG_589t1:c.*160C>A	NP_000109.1:n.*160C>A
NM_001114753.2:c.1902C>A , LRG_589t2:c.1902C>A	NP_001108225.1:p.Ser634=
NM_001278138.1:c.1356C>A	NP_001265067.1:p.Ser452=
NM_001114753.3:c.1902C>A MANE Select	NP_001108225.1:p.Ser634=
NM_001278138.2:c.1356C>A	NP_001265067.1:p.Ser452=