Canonical Allele Identifier: CA341752581

Gene: AMPD1

Linked Data

• dbSNP Id: rs1658245923
• MyVariant Identifiers: chr1:g.115226896C>A (hg19) ; chr1:g.114684275C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114684275C>A , CM000663.2:g.114684275C>A	GRCh38
NC_000001.10:g.115226896C>A , CM000663.1:g.115226896C>A	GRCh37
NC_000001.9:g.115028419C>A	NCBI36
NG_008012.1:g.16281G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369538.4:c.459G>T	ENSP00000358551.4:p.Arg153Ser
ENST00000520113.7:c.471G>T MANE Select	ENSP00000430075.3:p.Arg157Ser
ENST00000637080.1:c.474G>T	ENSP00000489753.1:p.Arg158Ser
ENST00000639077.1:n.136G>T
ENST00000369538.3:c.558G>T	ENSP00000358551.3:p.Arg186Ser
ENST00000485564.3:n.345G>T
ENST00000520113.6:c.570G>T	ENSP00000430075.2:p.Arg190Ser
NM_000036.2:c.570G>T	NP_000027.2:p.Arg190Ser
NM_001172626.1:c.558G>T	NP_001166097.1:p.Arg186Ser
NM_000036.3:c.471G>T MANE Select	NP_000027.3:p.Arg157Ser
NM_001172626.2:c.459G>T	NP_001166097.2:p.Arg153Ser