Canonical Allele Identifier: CA341748629

Gene: AMPD1

Linked Data

• MyVariant Identifiers: chr1:g.115220074T>G (hg19) ; chr1:g.114677453T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114677453T>G , CM000663.2:g.114677453T>G	GRCh38
NC_000001.10:g.115220074T>G , CM000663.1:g.115220074T>G	GRCh37
NC_000001.9:g.115021597T>G	NCBI36
NG_008012.1:g.23103A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369538.4:c.1274A>C	ENSP00000358551.4:p.Tyr425Ser
ENST00000520113.7:c.1286A>C MANE Select	ENSP00000430075.3:p.Tyr429Ser
ENST00000637080.1:c.1069A>C	ENSP00000489753.1:n.1069A>C
ENST00000639077.1:n.951A>C
ENST00000369538.3:c.1373A>C	ENSP00000358551.3:p.Tyr458Ser
ENST00000520113.6:c.1385A>C	ENSP00000430075.2:p.Tyr462Ser
NM_000036.2:c.1385A>C	NP_000027.2:p.Tyr462Ser
NM_001172626.1:c.1373A>C	NP_001166097.1:p.Tyr458Ser
NM_000036.3:c.1286A>C MANE Select	NP_000027.3:p.Tyr429Ser
NM_001172626.2:c.1274A>C	NP_001166097.2:p.Tyr425Ser