Canonical Allele Identifier: CA341749098

Gene: AMPD1

Linked Data

• COSMIC: COSM159043 ; COSM4810116
• MyVariant Identifiers: chr1:g.115220601C>G (hg19) ; chr1:g.114677980C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114677980C>G , CM000663.2:g.114677980C>G	GRCh38
NC_000001.10:g.115220601C>G , CM000663.1:g.115220601C>G	GRCh37
NC_000001.9:g.115022124C>G	NCBI36
NG_008012.1:g.22576G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000369538.4:c.1142G>C	ENSP00000358551.4:p.Ser381Thr
ENST00000520113.7:c.1154G>C MANE Select	ENSP00000430075.3:p.Ser385Thr
ENST00000637080.1:c.937G>C	ENSP00000489753.1:n.937G>C
ENST00000639077.1:n.819G>C
ENST00000369538.3:c.1241G>C	ENSP00000358551.3:p.Ser414Thr
ENST00000520113.6:c.1253G>C	ENSP00000430075.2:p.Ser418Thr
NM_000036.2:c.1253G>C	NP_000027.2:p.Ser418Thr
NM_001172626.1:c.1241G>C	NP_001166097.1:p.Ser414Thr
NM_000036.3:c.1154G>C MANE Select	NP_000027.3:p.Ser385Thr
NM_001172626.2:c.1142G>C	NP_001166097.2:p.Ser381Thr