Canonical Allele Identifier: CA423904892

Gene: EGLN1

Linked Data

• MyVariant Identifiers: chr1:g.231506343G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.231370597G>T , CM000663.2:g.231370597G>T	GRCh38
NC_000001.10:g.231506343G>T , CM000663.1:g.231506343G>T	GRCh37
NC_000001.9:g.229572966G>T	NCBI36
NG_015865.1:g.59448C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366641.4:c.1113C>A MANE Select	ENSP00000355601.3:p.Arg371=
ENST00000476717.2:n.390C>A
ENST00000653198.1:n.655C>A
ENST00000653908.1:c.151-2961C>A	ENSP00000499669.1:n.151-2961C>A
ENST00000654803.1:c.335C>A
ENST00000658954.1:c.487C>A
ENST00000662216.1:c.252C>A	ENSP00000499467.1:p.Arg84=
ENST00000663780.1:n.213C>A
ENST00000667629.1:c.316-2961C>A	ENSP00000499629.1:n.316-2961C>A
ENST00000670301.1:c.230-4122C>A
ENST00000366641.3:c.1113C>A	ENSP00000355601.3:p.Arg371=
ENST00000476717.1:n.390C>A
NM_022051.2:c.1113C>A	NP_071334.1:p.Arg371=
XM_005273166.3:c.1113C>A	XP_005273223.1:p.Arg371=
XM_005273167.3:c.1012-2961C>A	XP_005273224.1:n.1012-2961C>A
XM_005273166.5:c.1113C>A	XP_005273223.1:p.Arg371=
XM_005273167.5:c.1012-2961C>A	XP_005273224.1:n.1012-2961C>A
XM_024447734.1:c.1012-2961C>A	XP_024303502.1:n.1012-2961C>A
NM_001377260.1:c.1113C>A	NP_001364189.1:p.Arg371=
NM_001377261.1:c.1012-2961C>A	NP_001364190.1:n.1012-2961C>A
NM_022051.3:c.1113C>A MANE Select	NP_071334.1:p.Arg371=