Canonical Allele Identifier: CA341748705

Gene: AMPD1

Linked Data

• MyVariant Identifiers: chr1:g.115220103G>T (hg19) ; chr1:g.114677482G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114677482G>T , CM000663.2:g.114677482G>T	GRCh38
NC_000001.10:g.115220103G>T , CM000663.1:g.115220103G>T	GRCh37
NC_000001.9:g.115021626G>T	NCBI36
NG_008012.1:g.23074C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369538.4:c.1245C>A	ENSP00000358551.4:p.Tyr415Ter
ENST00000520113.7:c.1257C>A MANE Select	ENSP00000430075.3:p.Tyr419Ter
ENST00000637080.1:c.1040C>A	ENSP00000489753.1:n.1040C>A
ENST00000639077.1:n.922C>A
ENST00000369538.3:c.1344C>A	ENSP00000358551.3:p.Tyr448Ter
ENST00000520113.6:c.1356C>A	ENSP00000430075.2:p.Tyr452Ter
NM_000036.2:c.1356C>A	NP_000027.2:p.Tyr452Ter
NM_001172626.1:c.1344C>A	NP_001166097.1:p.Tyr448Ter
NM_000036.3:c.1257C>A MANE Select	NP_000027.3:p.Tyr419Ter
NM_001172626.2:c.1245C>A	NP_001166097.2:p.Tyr415Ter