Canonical Allele Identifier: CA407040825

Gene: KLK4

Linked Data

• MyVariant Identifiers: chr19:g.51411716A>T (hg19) ; chr19:g.50908460A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908460A>T , CM000681.2:g.50908460A>T	GRCh38
NC_000019.9:g.51411716A>T , CM000681.1:g.51411716A>T	GRCh37
NC_000019.8:g.56103528A>T	NCBI36
NG_012154.2:g.7279T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.511T>A MANE Select	ENSP00000326159.1:p.Ser171Thr
ENST00000324041.5:c.511T>A	ENSP00000326159.1:p.Ser171Thr
ENST00000431178.2:c.328+119T>A	ENSP00000399448.2:n.328+119T>A
ENST00000593885.1:c.*6T>A	ENSP00000469769.1:n.*6T>A
ENST00000596876.1:n.513T>A
ENST00000598305.5:c.*6T>A	ENSP00000469963.1:n.*6T>A
ENST00000599865.5:n.447T>A
ENST00000602148.1:c.523T>A	ENSP00000472091.1:n.523T>A
NM_001302961.1:c.226T>A	NP_001289890.1:p.Ser76Thr
NM_004917.4:c.511T>A	NP_004908.4:p.Ser171Thr
NR_126566.1:n.500T>A
XM_005259441.3:c.226T>A	XP_005259498.2:p.Ser76Thr
XM_011527545.1:c.*6T>A	XP_011525847.1:n.*6T>A
XM_011527546.1:c.475+119T>A	XP_011525848.1:n.475+119T>A
XM_011527547.1:c.364T>A	XP_011525849.1:p.Ser122Thr
XM_005259441.4:c.226T>A	XP_005259498.2:p.Ser76Thr
XM_011527545.3:c.*6T>A	XP_011525847.1:n.*6T>A
XM_011527546.2:c.475+119T>A	XP_011525848.1:n.475+119T>A
NM_001302961.2:c.226T>A	NP_001289890.1:p.Ser76Thr
NR_126566.2:n.500T>A
NM_004917.5:c.511T>A MANE Select	NP_004908.4:p.Ser171Thr