Canonical Allele Identifier: CA341749109

Gene: AMPD1

Linked Data

• MyVariant Identifiers: chr1:g.115220607C>G (hg19) ; chr1:g.114677986C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114677986C>G , CM000663.2:g.114677986C>G	GRCh38
NC_000001.10:g.115220607C>G , CM000663.1:g.115220607C>G	GRCh37
NC_000001.9:g.115022130C>G	NCBI36
NG_008012.1:g.22570G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000369538.4:c.1136G>C	ENSP00000358551.4:p.Gly379Ala
ENST00000520113.7:c.1148G>C MANE Select	ENSP00000430075.3:p.Gly383Ala
ENST00000637080.1:c.931G>C	ENSP00000489753.1:n.931G>C
ENST00000639077.1:n.813G>C
ENST00000369538.3:c.1235G>C	ENSP00000358551.3:p.Gly412Ala
ENST00000520113.6:c.1247G>C	ENSP00000430075.2:p.Gly416Ala
NM_000036.2:c.1247G>C	NP_000027.2:p.Gly416Ala
NM_001172626.1:c.1235G>C	NP_001166097.1:p.Gly412Ala
NM_000036.3:c.1148G>C MANE Select	NP_000027.3:p.Gly383Ala
NM_001172626.2:c.1136G>C	NP_001166097.2:p.Gly379Ala