Canonical Allele Identifier: CA341748501

Gene: AMPD1

Linked Data

• MyVariant Identifiers: chr1:g.115220038G>T (hg19) ; chr1:g.114677417G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114677417G>T , CM000663.2:g.114677417G>T	GRCh38
NC_000001.10:g.115220038G>T , CM000663.1:g.115220038G>T	GRCh37
NC_000001.9:g.115021561G>T	NCBI36
NG_008012.1:g.23139C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369538.4:c.1310C>A	ENSP00000358551.4:p.Ser437Tyr
ENST00000520113.7:c.1322C>A MANE Select	ENSP00000430075.3:p.Ser441Tyr
ENST00000637080.1:c.1105C>A	ENSP00000489753.1:n.1105C>A
ENST00000639077.1:n.987C>A
ENST00000369538.3:c.1409C>A	ENSP00000358551.3:p.Ser470Tyr
ENST00000520113.6:c.1421C>A	ENSP00000430075.2:p.Ser474Tyr
NM_000036.2:c.1421C>A	NP_000027.2:p.Ser474Tyr
NM_001172626.1:c.1409C>A	NP_001166097.1:p.Ser470Tyr
NM_000036.3:c.1322C>A MANE Select	NP_000027.3:p.Ser441Tyr
NM_001172626.2:c.1310C>A	NP_001166097.2:p.Ser437Tyr