Canonical Allele Identifier: CA508313891

Gene: KLK4

Linked Data

• MyVariant Identifiers: chr19:g.51411860A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908604A>C , CM000681.2:g.50908604A>C	GRCh38
NC_000019.9:g.51411860A>C , CM000681.1:g.51411860A>C	GRCh37
NC_000019.8:g.56103672A>C	NCBI36
NG_012154.2:g.7135T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000324041.6:c.450T>G MANE Select	ENSP00000326159.1:p.Val150=
ENST00000324041.5:c.450T>G	ENSP00000326159.1:p.Val150=
ENST00000431178.2:c.303T>G	ENSP00000399448.2:p.Val101=
ENST00000593885.1:c.165T>G	ENSP00000469769.1:p.Val55=
ENST00000596876.1:n.369T>G
ENST00000598305.5:c.165T>G	ENSP00000469963.1:p.Val55=
ENST00000599865.5:n.303T>G
ENST00000602148.1:c.462T>G	ENSP00000472091.1:n.462T>G
NM_001302961.1:c.165T>G	NP_001289890.1:p.Val55=
NM_004917.4:c.450T>G	NP_004908.4:p.Val150=
NR_126566.1:n.443T>G
XM_005259441.3:c.165T>G	XP_005259498.2:p.Val55=
XM_011527545.1:c.450T>G	XP_011525847.1:p.Val150=
XM_011527546.1:c.450T>G	XP_011525848.1:p.Val150=
XM_011527547.1:c.303T>G	XP_011525849.1:p.Val101=
XM_005259441.4:c.165T>G	XP_005259498.2:p.Val55=
XM_011527545.3:c.450T>G	XP_011525847.1:p.Val150=
XM_011527546.2:c.450T>G	XP_011525848.1:p.Val150=
NM_001302961.2:c.165T>G	NP_001289890.1:p.Val55=
NR_126566.2:n.443T>G
NM_004917.5:c.450T>G MANE Select	NP_004908.4:p.Val150=