Canonical Allele Identifier: CA419883000

Gene: AMPD1

Linked Data

• MyVariant Identifiers: chr1:g.115220016G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114677395G>T , CM000663.2:g.114677395G>T	GRCh38
NC_000001.10:g.115220016G>T , CM000663.1:g.115220016G>T	GRCh37
NC_000001.9:g.115021539G>T	NCBI36
NG_008012.1:g.23161C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369538.4:c.1332C>A	ENSP00000358551.4:p.Ile444=
ENST00000520113.7:c.1344C>A MANE Select	ENSP00000430075.3:p.Ile448=
ENST00000637080.1:c.1127C>A	ENSP00000489753.1:n.1127C>A
ENST00000639077.1:n.1009C>A
ENST00000369538.3:c.1431C>A	ENSP00000358551.3:p.Ile477=
ENST00000520113.6:c.1443C>A	ENSP00000430075.2:p.Ile481=
NM_000036.2:c.1443C>A	NP_000027.2:p.Ile481=
NM_001172626.1:c.1431C>A	NP_001166097.1:p.Ile477=
NM_000036.3:c.1344C>A MANE Select	NP_000027.3:p.Ile448=
NM_001172626.2:c.1332C>A	NP_001166097.2:p.Ile444=