Canonical Allele Identifier: CA424040858

Gene: EGLN1

Linked Data

• gnomAD v4: 1-231421883-G-T
• MyVariant Identifiers: chr1:g.231557629G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.231421883G>T , CM000663.2:g.231421883G>T	GRCh38
NC_000001.10:g.231557629G>T , CM000663.1:g.231557629G>T	GRCh37
NC_000001.9:g.229624252G>T	NCBI36
NG_015865.1:g.8162C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000366641.4:c.6C>A MANE Select	ENSP00000355601.3:p.Ala2=
ENST00000653198.1:n.433+40589C>A
ENST00000653908.1:c.30+40555C>A	ENSP00000499669.1:n.30+40555C>A
ENST00000662216.1:c.30+40555C>A	ENSP00000499467.1:n.30+40555C>A
ENST00000366641.3:c.6C>A	ENSP00000355601.3:p.Ala2=
NM_022051.2:c.6C>A	NP_071334.1:p.Ala2=
XM_005273166.3:c.6C>A	XP_005273223.1:p.Ala2=
XM_005273167.3:c.6C>A	XP_005273224.1:p.Ala2=
XM_005273166.5:c.6C>A	XP_005273223.1:p.Ala2=
XM_005273167.5:c.6C>A	XP_005273224.1:p.Ala2=
XM_024447734.1:c.6C>A	XP_024303502.1:p.Ala2=
NM_001377260.1:c.6C>A	NP_001364189.1:p.Ala2=
NM_001377261.1:c.6C>A	NP_001364190.1:p.Ala2=
NM_022051.3:c.6C>A MANE Select	NP_071334.1:p.Ala2=