Canonical Allele Identifier: CA392730185

Gene: CA12

Linked Data

• dbSNP Id: rs1329647552
• gnomAD v2: 15-63637684-C-T
• gnomAD v4: 15-63345485-C-T
• MyVariant Identifiers: chr15:g.63637684C>T (hg19) ; chr15:g.63345485C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.63345485C>T , CM000677.2:g.63345485C>T	GRCh38
NC_000015.9:g.63637684C>T , CM000677.1:g.63637684C>T	GRCh37
NC_000015.8:g.61424737C>T	NCBI36
NG_028022.1:g.41392G>A
NG_028022.2:g.41682G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000178638.8:c.421G>A MANE Select	ENSP00000178638.3:p.Ala141Thr
ENST00000178638.7:c.421G>A	ENSP00000178638.3:p.Ala141Thr
ENST00000344366.7:c.421G>A	ENSP00000343088.3:p.Ala141Thr
ENST00000422263.2:c.241G>A	ENSP00000403028.2:p.Ala81Thr
NM_001218.4:c.421G>A	NP_001209.1:p.Ala141Thr
NM_001293642.1:c.241G>A	NP_001280571.1:p.Ala81Thr
NM_206925.2:c.421G>A	NP_996808.1:p.Ala141Thr
NR_135511.1:n.914G>A
NM_001218.5:c.421G>A MANE Select	NP_001209.1:p.Ala141Thr
NR_135511.2:n.594G>A
NM_001293642.2:c.241G>A	NP_001280571.1:p.Ala81Thr
NM_206925.3:c.421G>A	NP_996808.1:p.Ala141Thr