Canonical Allele Identifier: CA508313886

Gene: KLK4

Linked Data

• MyVariant Identifiers: chr19:g.51411854G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908598G>T , CM000681.2:g.50908598G>T	GRCh38
NC_000019.9:g.51411854G>T , CM000681.1:g.51411854G>T	GRCh37
NC_000019.8:g.56103666G>T	NCBI36
NG_012154.2:g.7141C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000324041.6:c.456C>A MANE Select	ENSP00000326159.1:p.Gly152=
ENST00000324041.5:c.456C>A	ENSP00000326159.1:p.Gly152=
ENST00000431178.2:c.309C>A	ENSP00000399448.2:p.Gly103=
ENST00000593885.1:c.171C>A	ENSP00000469769.1:p.Gly57=
ENST00000596876.1:n.375C>A
ENST00000598305.5:c.171C>A	ENSP00000469963.1:p.Gly57=
ENST00000599865.5:n.309C>A
ENST00000602148.1:c.468C>A	ENSP00000472091.1:n.468C>A
NM_001302961.1:c.171C>A	NP_001289890.1:p.Gly57=
NM_004917.4:c.456C>A	NP_004908.4:p.Gly152=
NR_126566.1:n.449C>A
XM_005259441.3:c.171C>A	XP_005259498.2:p.Gly57=
XM_011527545.1:c.456C>A	XP_011525847.1:p.Gly152=
XM_011527546.1:c.456C>A	XP_011525848.1:p.Gly152=
XM_011527547.1:c.309C>A	XP_011525849.1:p.Gly103=
XM_005259441.4:c.171C>A	XP_005259498.2:p.Gly57=
XM_011527545.3:c.456C>A	XP_011525847.1:p.Gly152=
XM_011527546.2:c.456C>A	XP_011525848.1:p.Gly152=
NM_001302961.2:c.171C>A	NP_001289890.1:p.Gly57=
NR_126566.2:n.449C>A
NM_004917.5:c.456C>A MANE Select	NP_004908.4:p.Gly152=