Canonical Allele Identifier: CA2264701176

Gene: CA10

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.51882949T>G , CM000679.2:g.51882949T>G	GRCh38
NC_000017.10:g.49960309T>G , CM000679.1:g.49960309T>G	GRCh37
NC_000017.9:g.47315308T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000451037.7:c.279+48041A>C MANE Select	ENSP00000405388.2:n.279+48041A>C
ENST00000285273.8:c.279+48041A>C	ENSP00000285273.4:n.279+48041A>C
ENST00000442502.6:c.279+48041A>C	ENSP00000390666.2:n.279+48041A>C
ENST00000451037.6:c.279+48041A>C	ENSP00000405388.2:n.279+48041A>C
ENST00000570565.5:c.54+48041A>C	ENSP00000459619.1:n.54+48041A>C
ENST00000571371.5:c.*321+48041A>C	ENSP00000461908.1:n.*321+48041A>C
ENST00000575181.1:c.279+48041A>C	ENSP00000460238.1:n.279+48041A>C
NM_001082533.1:c.279+48041A>C	NP_001076002.1:n.279+48041A>C
NM_001082534.1:c.279+48041A>C	NP_001076003.1:n.279+48041A>C
NM_020178.4:c.279+48041A>C	NP_064563.1:n.279+48041A>C
NM_020178.5:c.279+48041A>C MANE Select	NP_064563.1:n.279+48041A>C
NM_001082534.2:c.279+48041A>C	NP_001076003.1:n.279+48041A>C