Canonical Allele Identifier: CA341752355

Gene: AMPD1

Linked Data

• MyVariant Identifiers: chr1:g.115226844C>G (hg19) ; chr1:g.114684223C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114684223C>G , CM000663.2:g.114684223C>G	GRCh38
NC_000001.10:g.115226844C>G , CM000663.1:g.115226844C>G	GRCh37
NC_000001.9:g.115028367C>G	NCBI36
NG_008012.1:g.16333G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369538.4:c.511G>C	ENSP00000358551.4:p.Val171Leu
ENST00000520113.7:c.523G>C MANE Select	ENSP00000430075.3:p.Val175Leu
ENST00000637080.1:c.526G>C	ENSP00000489753.1:p.Val176Leu
ENST00000639077.1:n.188G>C
ENST00000369538.3:c.610G>C	ENSP00000358551.3:p.Val204Leu
ENST00000485564.3:n.397G>C
ENST00000520113.6:c.622G>C	ENSP00000430075.2:p.Val208Leu
NM_000036.2:c.622G>C	NP_000027.2:p.Val208Leu
NM_001172626.1:c.610G>C	NP_001166097.1:p.Val204Leu
NM_000036.3:c.523G>C MANE Select	NP_000027.3:p.Val175Leu
NM_001172626.2:c.511G>C	NP_001166097.2:p.Val171Leu