Canonical Allele Identifier: CA341752565

Gene: AMPD1

Linked Data

• MyVariant Identifiers: chr1:g.115226892G>A (hg19) ; chr1:g.114684271G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114684271G>A , CM000663.2:g.114684271G>A	GRCh38
NC_000001.10:g.115226892G>A , CM000663.1:g.115226892G>A	GRCh37
NC_000001.9:g.115028415G>A	NCBI36
NG_008012.1:g.16285C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369538.4:c.463C>T	ENSP00000358551.4:p.Pro155Ser
ENST00000520113.7:c.475C>T MANE Select	ENSP00000430075.3:p.Pro159Ser
ENST00000637080.1:c.478C>T	ENSP00000489753.1:p.Pro160Ser
ENST00000639077.1:n.140C>T
ENST00000369538.3:c.562C>T	ENSP00000358551.3:p.Pro188Ser
ENST00000485564.3:n.349C>T
ENST00000520113.6:c.574C>T	ENSP00000430075.2:p.Pro192Ser
NM_000036.2:c.574C>T	NP_000027.2:p.Pro192Ser
NM_001172626.1:c.562C>T	NP_001166097.1:p.Pro188Ser
NM_000036.3:c.475C>T MANE Select	NP_000027.3:p.Pro159Ser
NM_001172626.2:c.463C>T	NP_001166097.2:p.Pro155Ser