Canonical Allele Identifier: CA2341201979

Gene: KLK12

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.51034426C>T , CM000681.2:g.51034426C>T	GRCh38
NC_000019.9:g.51537682C>T , CM000681.1:g.51537682C>T	GRCh37
NC_000019.8:g.56229494C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684732.1:c.37+159G>A MANE Select	ENSP00000508282.1:n.37+159G>A
ENST00000250351.4:c.37+159G>A	ENSP00000250351.4:n.37+159G>A
ENST00000319590.8:c.37+159G>A	ENSP00000324181.4:n.37+159G>A
ENST00000525263.5:c.37+159G>A	ENSP00000436458.1:n.37+159G>A
ENST00000526824.5:c.196G>A	ENSP00000434604.1:p.Gly66Arg
ENST00000529888.5:c.37+159G>A	ENSP00000434036.1:n.37+159G>A
ENST00000530943.6:c.196G>A	ENSP00000434339.1:p.Gly66Arg
ENST00000531374.5:c.37+159G>A	ENSP00000436121.1:n.37+159G>A
NM_019598.2:c.37+159G>A	NP_062544.1:n.37+159G>A
NM_145894.1:c.37+159G>A	NP_665901.1:n.37+159G>A
NM_145895.1:c.37+159G>A	NP_665902.1:n.37+159G>A
XM_005258950.2:c.-35G>A	XP_005259007.1:n.-35G>A
XM_005258951.2:c.37+159G>A	XP_005259008.1:n.37+159G>A
XM_005258950.4:c.-35G>A	XP_005259007.1:n.-35G>A
XM_005258951.3:c.37+159G>A	XP_005259008.1:n.37+159G>A
NM_001370125.1:c.37+159G>A MANE Select	NP_001357054.1:n.37+159G>A
NM_001370126.1:c.-35G>A	NP_001357055.1:n.-35G>A
NM_001370127.1:c.-34+159G>A	NP_001357056.1:n.-34+159G>A
NM_001370128.1:c.-35G>A	NP_001357057.1:n.-35G>A
NM_019598.3:c.37+159G>A	NP_062544.1:n.37+159G>A
NM_145894.2:c.37+159G>A	NP_665901.1:n.37+159G>A
NM_145895.2:c.-34+159G>A	NP_665902.2:n.-34+159G>A