Canonical Allele Identifier: CA1142888950

Gene: EGLN1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.231421877G= , CM000663.2:g.231421877G=	GRCh38
NC_000001.10:g.231557623G= , CM000663.1:g.231557623G=	GRCh37
NC_000001.9:g.229624246G=	NCBI36
NG_015865.1:g.8168C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000366641.4:c.12C= MANE Select	ENSP00000355601.3:p.Asp4=
ENST00000653198.1:n.433+40595C=
ENST00000653908.1:c.30+40561C=	ENSP00000499669.1:n.30+40561C=
ENST00000662216.1:c.30+40561C=	ENSP00000499467.1:n.30+40561C=
ENST00000366641.3:c.12C=	ENSP00000355601.3:p.Asp4=
NM_022051.2:c.12C=	NP_071334.1:p.Asp4=
XM_005273166.3:c.12C=	XP_005273223.1:p.Asp4=
XM_005273167.3:c.12C=	XP_005273224.1:p.Asp4=
XM_005273166.5:c.12C=	XP_005273223.1:p.Asp4=
XM_005273167.5:c.12C=	XP_005273224.1:p.Asp4=
XM_024447734.1:c.12C=	XP_024303502.1:p.Asp4=
NM_001377260.1:c.12C=	NP_001364189.1:p.Asp4=
NM_001377261.1:c.12C=	NP_001364190.1:p.Asp4=
NM_022051.3:c.12C= MANE Select	NP_071334.1:p.Asp4=