Canonical Allele Identifier: CA508313986

Gene: KLK4

Linked Data

• MyVariant Identifiers: chr19:g.51411976A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908720A>G , CM000681.2:g.50908720A>G	GRCh38
NC_000019.9:g.51411976A>G , CM000681.1:g.51411976A>G	GRCh37
NC_000019.8:g.56103788A>G	NCBI36
NG_012154.2:g.7019T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.334T>C MANE Select	ENSP00000326159.1:p.Leu112=
ENST00000324041.5:c.334T>C	ENSP00000326159.1:p.Leu112=
ENST00000431178.2:c.187T>C	ENSP00000399448.2:p.Leu63=
ENST00000593885.1:c.49T>C	ENSP00000469769.1:p.Leu17=
ENST00000596876.1:n.253T>C
ENST00000598305.5:c.49T>C	ENSP00000469963.1:p.Leu17=
ENST00000599865.5:n.187T>C
ENST00000602148.1:c.346T>C	ENSP00000472091.1:n.346T>C
NM_001302961.1:c.49T>C	NP_001289890.1:p.Leu17=
NM_004917.4:c.334T>C	NP_004908.4:p.Leu112=
NR_126566.1:n.327T>C
XM_005259441.3:c.49T>C	XP_005259498.2:p.Leu17=
XM_011527545.1:c.334T>C	XP_011525847.1:p.Leu112=
XM_011527546.1:c.334T>C	XP_011525848.1:p.Leu112=
XM_011527547.1:c.187T>C	XP_011525849.1:p.Leu63=
XM_005259441.4:c.49T>C	XP_005259498.2:p.Leu17=
XM_011527545.3:c.334T>C	XP_011525847.1:p.Leu112=
XM_011527546.2:c.334T>C	XP_011525848.1:p.Leu112=
NM_001302961.2:c.49T>C	NP_001289890.1:p.Leu17=
NR_126566.2:n.327T>C
NM_004917.5:c.334T>C MANE Select	NP_004908.4:p.Leu112=