Canonical Allele Identifier: CA1226942673
Gene: EGLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.231370591A= , CM000663.2:g.231370591A= GRCh38
NC_000001.10:g.231506337A= , CM000663.1:g.231506337A= GRCh37
NC_000001.9:g.229572960A= NCBI36
NG_015865.1:g.59454T=

Transcript Alleles

HGVS Amino-acid change
ENST00000366641.4:c.1119T= MANE Select ENSP00000355601.3:p.Pro373=
ENST00000476717.2:n.396T=
ENST00000653198.1:n.661T=
ENST00000653908.1:c.151-2955T= ENSP00000499669.1:n.151-2955T=
ENST00000654803.1:c.341T=
ENST00000658954.1:c.493T=
ENST00000662216.1:c.258T= ENSP00000499467.1:p.Pro86=
ENST00000663780.1:n.219T=
ENST00000667629.1:c.316-2955T= ENSP00000499629.1:n.316-2955T=
ENST00000670301.1:c.230-4116T=
ENST00000366641.3:c.1119T= ENSP00000355601.3:p.Pro373=
ENST00000476717.1:n.396T=
NM_022051.2:c.1119T= NP_071334.1:p.Pro373=
XM_005273166.3:c.1119T= XP_005273223.1:p.Pro373=
XM_005273167.3:c.1012-2955T= XP_005273224.1:n.1012-2955T=
XM_005273166.5:c.1119T= XP_005273223.1:p.Pro373=
XM_005273167.5:c.1012-2955T= XP_005273224.1:n.1012-2955T=
XM_024447734.1:c.1012-2955T= XP_024303502.1:n.1012-2955T=
NM_001377260.1:c.1119T= NP_001364189.1:p.Pro373=
NM_001377261.1:c.1012-2955T= NP_001364190.1:n.1012-2955T=
NM_022051.3:c.1119T= MANE Select NP_071334.1:p.Pro373=