Canonical Allele Identifier: CA407040627

Gene: KLK4

Linked Data

• MyVariant Identifiers: chr19:g.51411682T>G (hg19) ; chr19:g.50908426T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908426T>G , CM000681.2:g.50908426T>G	GRCh38
NC_000019.9:g.51411682T>G , CM000681.1:g.51411682T>G	GRCh37
NC_000019.8:g.56103494T>G	NCBI36
NG_012154.2:g.7313A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.545A>C MANE Select	ENSP00000326159.1:p.Tyr182Ser
ENST00000324041.5:c.545A>C	ENSP00000326159.1:p.Tyr182Ser
ENST00000431178.2:c.328+153A>C	ENSP00000399448.2:n.328+153A>C
ENST00000593885.1:c.*40A>C	ENSP00000469769.1:n.*40A>C
ENST00000596876.1:n.547A>C
ENST00000598305.5:c.*40A>C	ENSP00000469963.1:n.*40A>C
ENST00000599865.5:n.481A>C
ENST00000602148.1:c.557A>C	ENSP00000472091.1:n.557A>C
NM_001302961.1:c.260A>C	NP_001289890.1:p.Tyr87Ser
NM_004917.4:c.545A>C	NP_004908.4:p.Tyr182Ser
NR_126566.1:n.534A>C
XM_005259441.3:c.260A>C	XP_005259498.2:p.Tyr87Ser
XM_011527545.1:c.*40A>C	XP_011525847.1:n.*40A>C
XM_011527546.1:c.475+153A>C	XP_011525848.1:n.475+153A>C
XM_011527547.1:c.398A>C	XP_011525849.1:p.Tyr133Ser
XM_005259441.4:c.260A>C	XP_005259498.2:p.Tyr87Ser
XM_011527545.3:c.*40A>C	XP_011525847.1:n.*40A>C
XM_011527546.2:c.475+153A>C	XP_011525848.1:n.475+153A>C
NM_001302961.2:c.260A>C	NP_001289890.1:p.Tyr87Ser
NR_126566.2:n.534A>C
NM_004917.5:c.545A>C MANE Select	NP_004908.4:p.Tyr182Ser