Canonical Allele Identifier: CA407041125

Gene: KLK4

Linked Data

• MyVariant Identifiers: chr19:g.51411729C>G (hg19) ; chr19:g.50908473C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908473C>G , CM000681.2:g.50908473C>G	GRCh38
NC_000019.9:g.51411729C>G , CM000681.1:g.51411729C>G	GRCh37
NC_000019.8:g.56103541C>G	NCBI36
NG_012154.2:g.7266G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.498G>C MANE Select	ENSP00000326159.1:p.Gln166His
ENST00000324041.5:c.498G>C	ENSP00000326159.1:p.Gln166His
ENST00000431178.2:c.328+106G>C	ENSP00000399448.2:n.328+106G>C
ENST00000593885.1:c.209G>C	ENSP00000469769.1:p.Ser70Thr
ENST00000596876.1:n.500G>C
ENST00000598305.5:c.209G>C	ENSP00000469963.1:p.Ser70Thr
ENST00000599865.5:n.434G>C
ENST00000602148.1:c.510G>C	ENSP00000472091.1:n.510G>C
NM_001302961.1:c.213G>C	NP_001289890.1:p.Gln71His
NM_004917.4:c.498G>C	NP_004908.4:p.Gln166His
NR_126566.1:n.487G>C
XM_005259441.3:c.213G>C	XP_005259498.2:p.Gln71His
XM_011527545.1:c.494G>C	XP_011525847.1:p.Ser165Thr
XM_011527546.1:c.475+106G>C	XP_011525848.1:n.475+106G>C
XM_011527547.1:c.351G>C	XP_011525849.1:p.Gln117His
XM_005259441.4:c.213G>C	XP_005259498.2:p.Gln71His
XM_011527545.3:c.494G>C	XP_011525847.1:p.Ser165Thr
XM_011527546.2:c.475+106G>C	XP_011525848.1:n.475+106G>C
NM_001302961.2:c.213G>C	NP_001289890.1:p.Gln71His
NR_126566.2:n.487G>C
NM_004917.5:c.498G>C MANE Select	NP_004908.4:p.Gln166His