Canonical Allele Identifier: CA9605107

Gene: KLK4

Linked Data

• dbSNP Id: rs747648672
• ExAC: 19:51412048 C / T
• gnomAD v2: 19-51412048-C-T
• MyVariant Identifiers: chr19:g.51412048C>T (hg19) ; chr19:g.50908792C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908792C>T , CM000681.2:g.50908792C>T	GRCh38
NC_000019.9:g.51412048C>T , CM000681.1:g.51412048C>T	GRCh37
NC_000019.8:g.56103860C>T	NCBI36
NG_012154.2:g.6947G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.262G>A MANE Select	ENSP00000326159.1:p.Ala88Thr
ENST00000324041.5:c.262G>A	ENSP00000326159.1:p.Ala88Thr
ENST00000431178.2:c.115G>A	ENSP00000399448.2:p.Ala39Thr
ENST00000593885.1:c.-24G>A	ENSP00000469769.1:n.-24G>A
ENST00000596876.1:n.181G>A
ENST00000598305.5:c.-24G>A	ENSP00000469963.1:n.-24G>A
ENST00000599865.5:n.115G>A
ENST00000602148.1:c.274G>A	ENSP00000472091.1:n.274G>A
NM_001302961.1:c.-24G>A	NP_001289890.1:n.-24G>A
NM_004917.4:c.262G>A	NP_004908.4:p.Ala88Thr
NR_126566.1:n.255G>A
XM_005259441.3:c.-24G>A	XP_005259498.2:n.-24G>A
XM_011527545.1:c.262G>A	XP_011525847.1:p.Ala88Thr
XM_011527546.1:c.262G>A	XP_011525848.1:p.Ala88Thr
XM_011527547.1:c.115G>A	XP_011525849.1:p.Ala39Thr
XM_005259441.4:c.-24G>A	XP_005259498.2:n.-24G>A
XM_011527545.3:c.262G>A	XP_011525847.1:p.Ala88Thr
XM_011527546.2:c.262G>A	XP_011525848.1:p.Ala88Thr
NM_001302961.2:c.-24G>A	NP_001289890.1:n.-24G>A
NR_126566.2:n.255G>A
NM_004917.5:c.262G>A MANE Select	NP_004908.4:p.Ala88Thr