Canonical Allele Identifier: CA407041858

Gene: KLK4

Linked Data

• dbSNP Id: rs1243253971
• gnomAD v2: 19-51412078-T-C
• gnomAD v4: 19-50908822-T-C
• MyVariant Identifiers: chr19:g.51412078T>C (hg19) ; chr19:g.50908822T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908822T>C , CM000681.2:g.50908822T>C	GRCh38
NC_000019.9:g.51412078T>C , CM000681.1:g.51412078T>C	GRCh37
NC_000019.8:g.56103890T>C	NCBI36
NG_012154.2:g.6917A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.232A>G MANE Select	ENSP00000326159.1:p.Thr78Ala
ENST00000324041.5:c.232A>G	ENSP00000326159.1:p.Thr78Ala
ENST00000431178.2:c.85A>G	ENSP00000399448.2:p.Thr29Ala
ENST00000593885.1:c.-54A>G	ENSP00000469769.1:n.-54A>G
ENST00000596876.1:n.151A>G
ENST00000598305.5:c.-54A>G	ENSP00000469963.1:n.-54A>G
ENST00000599865.5:n.85A>G
ENST00000602148.1:c.244A>G	ENSP00000472091.1:n.244A>G
NM_001302961.1:c.-54A>G	NP_001289890.1:n.-54A>G
NM_004917.4:c.232A>G	NP_004908.4:p.Thr78Ala
NR_126566.1:n.225A>G
XM_005259441.3:c.-54A>G	XP_005259498.2:n.-54A>G
XM_011527545.1:c.232A>G	XP_011525847.1:p.Thr78Ala
XM_011527546.1:c.232A>G	XP_011525848.1:p.Thr78Ala
XM_011527547.1:c.85A>G	XP_011525849.1:p.Thr29Ala
XM_005259441.4:c.-54A>G	XP_005259498.2:n.-54A>G
XM_011527545.3:c.232A>G	XP_011525847.1:p.Thr78Ala
XM_011527546.2:c.232A>G	XP_011525848.1:p.Thr78Ala
NM_001302961.2:c.-54A>G	NP_001289890.1:n.-54A>G
NR_126566.2:n.225A>G
NM_004917.5:c.232A>G MANE Select	NP_004908.4:p.Thr78Ala