Canonical Allele Identifier: CA241271
Community Standard Title: NM_000067.3(CA2):c.35-7C>A
Gene: CA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.85465265C>A , CM000670.2:g.85465265C>A GRCh38
NC_000008.10:g.86377494C>A , CM000670.1:g.86377494C>A GRCh37
NC_000008.9:g.86564746C>A NCBI36
NG_007287.1:g.6249C>A

Transcript Alleles

HGVS Amino-acid Change
NM_000067.3:c.35-7C>A MANE Select NP_000058.1:n.35-7C>A
ENST00000285379.10:c.35-7C>A MANE Select ENSP00000285379.4:n.35-7C>A
NM_000067.2:c.35-7C>A NP_000058.1:n.35-7C>A
NM_001293675.1:c.-150-7C>A NP_001280604.1:n.-150-7C>A
NM_001293675.2:c.-150-7C>A NP_001280604.1:n.-150-7C>A
ENST00000285379.9:c.35-7C>A ENSP00000285379.4:n.35-7C>A
ENST00000518231.1:n.106-7C>A
ENST00000520127.5:c.35-7C>A ENSP00000428443.1:n.35-7C>A
ENST00000520996.5:n.114-7C>A
ENST00000522742.1:c.35-7C>A ENSP00000428947.1:n.35-7C>A