Canonical Allele Identifier: CA508212014

Gene: KLK4

Linked Data

• MyVariant Identifiers: chr19:g.51411696G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908440G>C , CM000681.2:g.50908440G>C	GRCh38
NC_000019.9:g.51411696G>C , CM000681.1:g.51411696G>C	GRCh37
NC_000019.8:g.56103508G>C	NCBI36
NG_012154.2:g.7299C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.531C>G MANE Select	ENSP00000326159.1:p.Val177=
ENST00000324041.5:c.531C>G	ENSP00000326159.1:p.Val177=
ENST00000431178.2:c.328+139C>G	ENSP00000399448.2:n.328+139C>G
ENST00000593885.1:c.*26C>G	ENSP00000469769.1:n.*26C>G
ENST00000596876.1:n.533C>G
ENST00000598305.5:c.*26C>G	ENSP00000469963.1:n.*26C>G
ENST00000599865.5:n.467C>G
ENST00000602148.1:c.543C>G	ENSP00000472091.1:n.543C>G
NM_001302961.1:c.246C>G	NP_001289890.1:p.Val82=
NM_004917.4:c.531C>G	NP_004908.4:p.Val177=
NR_126566.1:n.520C>G
XM_005259441.3:c.246C>G	XP_005259498.2:p.Val82=
XM_011527545.1:c.*26C>G	XP_011525847.1:n.*26C>G
XM_011527546.1:c.475+139C>G	XP_011525848.1:n.475+139C>G
XM_011527547.1:c.384C>G	XP_011525849.1:p.Val128=
XM_005259441.4:c.246C>G	XP_005259498.2:p.Val82=
XM_011527545.3:c.*26C>G	XP_011525847.1:n.*26C>G
XM_011527546.2:c.475+139C>G	XP_011525848.1:n.475+139C>G
NM_001302961.2:c.246C>G	NP_001289890.1:p.Val82=
NR_126566.2:n.520C>G
NM_004917.5:c.531C>G MANE Select	NP_004908.4:p.Val177=