Canonical Allele Identifier: CA341752657

Gene: AMPD1

Linked Data

• MyVariant Identifiers: chr1:g.115226916T>G (hg19) ; chr1:g.114684295T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114684295T>G , CM000663.2:g.114684295T>G	GRCh38
NC_000001.10:g.115226916T>G , CM000663.1:g.115226916T>G	GRCh37
NC_000001.9:g.115028439T>G	NCBI36
NG_008012.1:g.16261A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369538.4:c.439A>C	ENSP00000358551.4:p.Met147Leu
ENST00000520113.7:c.451A>C MANE Select	ENSP00000430075.3:p.Met151Leu
ENST00000637080.1:c.454A>C	ENSP00000489753.1:p.Met152Leu
ENST00000639077.1:n.116A>C
ENST00000369538.3:c.538A>C	ENSP00000358551.3:p.Met180Leu
ENST00000485564.3:n.325A>C
ENST00000520113.6:c.550A>C	ENSP00000430075.2:p.Met184Leu
NM_000036.2:c.550A>C	NP_000027.2:p.Met184Leu
NM_001172626.1:c.538A>C	NP_001166097.1:p.Met180Leu
NM_000036.3:c.451A>C MANE Select	NP_000027.3:p.Met151Leu
NM_001172626.2:c.439A>C	NP_001166097.2:p.Met147Leu