Canonical Allele Identifier: CA1879974755

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127825316G= , CM000671.2:g.127825316G=	GRCh38
NC_000009.11:g.130587595G= , CM000671.1:g.130587595G=	GRCh37
NC_000009.10:g.129627416G=	NCBI36
NG_009551.1:g.34453C= , LRG_589:g.34453C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.185C=	ENSP00000479015.1:p.Pro62=
ENST00000373203.9:c.731C= MANE Select	ENSP00000362299.4:p.Pro244=
ENST00000344849.4:c.731C=	ENSP00000341917.3:p.Pro244=
ENST00000373203.8:c.731C=	ENSP00000362299.4:p.Pro244=
ENST00000480266.5:c.185C=	ENSP00000479015.1:p.Pro62=
NM_000118.3:c.731C= , LRG_589t1:c.731C=	NP_000109.1:p.Pro244=
NM_001114753.2:c.731C= , LRG_589t2:c.731C=	NP_001108225.1:p.Pro244=
NM_001278138.1:c.185C=	NP_001265067.1:p.Pro62=
NM_001114753.3:c.731C= MANE Select	NP_001108225.1:p.Pro244=
NM_001278138.2:c.185C=	NP_001265067.1:p.Pro62=