Canonical Allele Identifier: CA7602517

Gene: CA12

Linked Data

• dbSNP Id: rs771660006
• ExAC: 15:63637682 G / A
• gnomAD v2: 15-63637682-G-A
• gnomAD v3: 15-63345483-G-A
• gnomAD v4: 15-63345483-G-A
• MyVariant Identifiers: chr15:g.63637682G>A (hg19) ; chr15:g.63345483G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.63345483G>A , CM000677.2:g.63345483G>A	GRCh38
NC_000015.9:g.63637682G>A , CM000677.1:g.63637682G>A	GRCh37
NC_000015.8:g.61424735G>A	NCBI36
NG_028022.1:g.41394C>T
NG_028022.2:g.41684C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000178638.8:c.423C>T MANE Select	ENSP00000178638.3:p.Ala141=
ENST00000178638.7:c.423C>T	ENSP00000178638.3:p.Ala141=
ENST00000344366.7:c.423C>T	ENSP00000343088.3:p.Ala141=
ENST00000422263.2:c.243C>T	ENSP00000403028.2:p.Ala81=
NM_001218.4:c.423C>T	NP_001209.1:p.Ala141=
NM_001293642.1:c.243C>T	NP_001280571.1:p.Ala81=
NM_206925.2:c.423C>T	NP_996808.1:p.Ala141=
NR_135511.1:n.916C>T
NM_001218.5:c.423C>T MANE Select	NP_001209.1:p.Ala141=
NR_135511.2:n.596C>T
NM_001293642.2:c.243C>T	NP_001280571.1:p.Ala81=
NM_206925.3:c.423C>T	NP_996808.1:p.Ala141=