Canonical Allele Identifier: CA1879981957

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127829788G= , CM000671.2:g.127829788G=	GRCh38
NC_000009.11:g.130592067G= , CM000671.1:g.130592067G=	GRCh37
NC_000009.10:g.129631888G=	NCBI36
NG_009551.1:g.29981C= , LRG_589:g.29981C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001114753.3:c.259C= MANE Select	NP_001108225.1:p.Gln87=
ENST00000373203.9:c.259C= MANE Select	ENSP00000362299.4:p.Gln87=
NM_000118.3:c.259C= , LRG_589t1:c.259C=	NP_000109.1:p.Gln87=
NM_001114753.2:c.259C= , LRG_589t2:c.259C=	NP_001108225.1:p.Gln87=
NM_001278138.1:c.-288C=	NP_001265067.1:n.-288C=
NM_001278138.2:c.-288C=	NP_001265067.1:n.-288C=
ENST00000344849.4:c.259C=	ENSP00000341917.3:p.Gln87=
ENST00000373203.8:c.259C=	ENSP00000362299.4:p.Gln87=
ENST00000462196.1:n.17C=
ENST00000480266.5:c.-288C=	ENSP00000479015.1:n.-288C=
ENST00000480266.6:c.-288C=	ENSP00000479015.1:n.-288C=
XR_001746952.2:n.83-2610G=