Canonical Allele Identifier: CA14103884

Gene: CA12

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.63342206G>T , CM000677.2:g.63342206G>T	GRCh38
NC_000015.9:g.63634405G>T , CM000677.1:g.63634405G>T	GRCh37
NC_000015.8:g.61421458G>T	NCBI36
NG_028022.1:g.44671C>A
NG_028022.2:g.44961C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001218.5:c.430-109C>A MANE Select	NP_001209.1:n.430-109C>A
ENST00000178638.8:c.430-109C>A MANE Select	ENSP00000178638.3:n.430-109C>A
NM_001218.4:c.430-109C>A	NP_001209.1:n.430-109C>A
NM_001293642.1:c.250-109C>A	NP_001280571.1:n.250-109C>A
NM_001293642.2:c.250-109C>A	NP_001280571.1:n.250-109C>A
NM_206925.2:c.430-109C>A	NP_996808.1:n.430-109C>A
NM_206925.3:c.430-109C>A	NP_996808.1:n.430-109C>A
NR_135511.1:n.923-109C>A
NR_135511.2:n.603-109C>A
ENST00000178638.7:c.430-109C>A	ENSP00000178638.3:n.430-109C>A
ENST00000344366.7:c.430-109C>A	ENSP00000343088.3:n.430-109C>A
ENST00000422263.2:c.250-109C>A	ENSP00000403028.2:n.250-109C>A
XR_932358.1:n.875+285G>T