Canonical Allele Identifier: CA1157639587

Gene: CDA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.20618393T= , CM000663.2:g.20618393T=	GRCh38
NC_000001.10:g.20944886T= , CM000663.1:g.20944886T=	GRCh37
NC_000001.9:g.20817473T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000375071.4:c.325-59T= MANE Select	ENSP00000364212.3:n.325-59T=
ENST00000375071.3:c.325-59T=	ENSP00000364212.3:n.325-59T=
ENST00000461985.1:n.311-59T=
NM_001785.2:c.325-59T=	NP_001776.1:n.325-59T=
NM_001785.3:c.325-59T= MANE Select	NP_001776.1:n.325-59T=