Canonical Allele Identifier: CA374981732

Gene: ENG

Linked Data

• gnomAD v3: 9-127824423-C-A
• gnomAD v4: 9-127824423-C-A
• MyVariant Identifiers: chr9:g.130586702C>A (hg19) ; chr9:g.127824423C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127824423C>A , CM000671.2:g.127824423C>A	GRCh38
NC_000009.11:g.130586702C>A , CM000671.1:g.130586702C>A	GRCh37
NC_000009.10:g.129626523C>A	NCBI36
NG_009551.1:g.35346G>T , LRG_589:g.35346G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.469G>T	ENSP00000479015.1:p.Ala157Ser
ENST00000373203.9:c.1015G>T MANE Select	ENSP00000362299.4:p.Ala339Ser
ENST00000344849.4:c.1015G>T	ENSP00000341917.3:p.Ala339Ser
ENST00000373203.8:c.1015G>T	ENSP00000362299.4:p.Ala339Ser
ENST00000480266.5:c.469G>T	ENSP00000479015.1:p.Ala157Ser
NM_000118.3:c.1015G>T , LRG_589t1:c.1015G>T	NP_000109.1:p.Ala339Ser
NM_001114753.2:c.1015G>T , LRG_589t2:c.1015G>T	NP_001108225.1:p.Ala339Ser
NM_001278138.1:c.469G>T	NP_001265067.1:p.Ala157Ser
NM_001114753.3:c.1015G>T MANE Select	NP_001108225.1:p.Ala339Ser
NM_001278138.2:c.469G>T	NP_001265067.1:p.Ala157Ser