Canonical Allele Identifier: CA508313808

Gene: KLK4

Linked Data

• MyVariant Identifiers: chr19:g.51411977G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908721G>A , CM000681.2:g.50908721G>A	GRCh38
NC_000019.9:g.51411977G>A , CM000681.1:g.51411977G>A	GRCh37
NC_000019.8:g.56103789G>A	NCBI36
NG_012154.2:g.7018C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.333C>T MANE Select	ENSP00000326159.1:p.Pro111=
ENST00000324041.5:c.333C>T	ENSP00000326159.1:p.Pro111=
ENST00000431178.2:c.186C>T	ENSP00000399448.2:p.Pro62=
ENST00000593885.1:c.48C>T	ENSP00000469769.1:p.Pro16=
ENST00000596876.1:n.252C>T
ENST00000598305.5:c.48C>T	ENSP00000469963.1:p.Pro16=
ENST00000599865.5:n.186C>T
ENST00000602148.1:c.345C>T	ENSP00000472091.1:n.345C>T
NM_001302961.1:c.48C>T	NP_001289890.1:p.Pro16=
NM_004917.4:c.333C>T	NP_004908.4:p.Pro111=
NR_126566.1:n.326C>T
XM_005259441.3:c.48C>T	XP_005259498.2:p.Pro16=
XM_011527545.1:c.333C>T	XP_011525847.1:p.Pro111=
XM_011527546.1:c.333C>T	XP_011525848.1:p.Pro111=
XM_011527547.1:c.186C>T	XP_011525849.1:p.Pro62=
XM_005259441.4:c.48C>T	XP_005259498.2:p.Pro16=
XM_011527545.3:c.333C>T	XP_011525847.1:p.Pro111=
XM_011527546.2:c.333C>T	XP_011525848.1:p.Pro111=
NM_001302961.2:c.48C>T	NP_001289890.1:p.Pro16=
NR_126566.2:n.326C>T
NM_004917.5:c.333C>T MANE Select	NP_004908.4:p.Pro111=