Canonical Allele Identifier: CA1190281928

Gene: AMPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114684324T= , CM000663.2:g.114684324T=	GRCh38
NC_000001.10:g.115226945T= , CM000663.1:g.115226945T=	GRCh37
NC_000001.9:g.115028468T=	NCBI36
NG_008012.1:g.16232A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369538.4:c.410A=	ENSP00000358551.4:p.Tyr137=
ENST00000520113.7:c.422A= MANE Select	ENSP00000430075.3:p.Tyr141=
ENST00000637080.1:c.425A=	ENSP00000489753.1:p.Tyr142=
ENST00000639077.1:n.87A=
ENST00000369538.3:c.509A=	ENSP00000358551.3:p.Tyr170=
ENST00000485564.3:n.296A=
ENST00000520113.6:c.521A=	ENSP00000430075.2:p.Tyr174=
NM_000036.2:c.521A=	NP_000027.2:p.Tyr174=
NM_001172626.1:c.509A=	NP_001166097.1:p.Tyr170=
NM_000036.3:c.422A= MANE Select	NP_000027.3:p.Tyr141=
NM_001172626.2:c.410A=	NP_001166097.2:p.Tyr137=