Canonical Allele Identifier: CA407041335

Gene: KLK4

Linked Data

• MyVariant Identifiers: chr19:g.51411864A>C (hg19) ; chr19:g.50908608A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908608A>C , CM000681.2:g.50908608A>C	GRCh38
NC_000019.9:g.51411864A>C , CM000681.1:g.51411864A>C	GRCh37
NC_000019.8:g.56103676A>C	NCBI36
NG_012154.2:g.7131T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000324041.6:c.446T>G MANE Select	ENSP00000326159.1:p.Leu149Arg
ENST00000324041.5:c.446T>G	ENSP00000326159.1:p.Leu149Arg
ENST00000431178.2:c.299T>G	ENSP00000399448.2:p.Leu100Arg
ENST00000593885.1:c.161T>G	ENSP00000469769.1:p.Leu54Arg
ENST00000596876.1:n.365T>G
ENST00000598305.5:c.161T>G	ENSP00000469963.1:p.Leu54Arg
ENST00000599865.5:n.299T>G
ENST00000602148.1:c.458T>G	ENSP00000472091.1:n.458T>G
NM_001302961.1:c.161T>G	NP_001289890.1:p.Leu54Arg
NM_004917.4:c.446T>G	NP_004908.4:p.Leu149Arg
NR_126566.1:n.439T>G
XM_005259441.3:c.161T>G	XP_005259498.2:p.Leu54Arg
XM_011527545.1:c.446T>G	XP_011525847.1:p.Leu149Arg
XM_011527546.1:c.446T>G	XP_011525848.1:p.Leu149Arg
XM_011527547.1:c.299T>G	XP_011525849.1:p.Leu100Arg
XM_005259441.4:c.161T>G	XP_005259498.2:p.Leu54Arg
XM_011527545.3:c.446T>G	XP_011525847.1:p.Leu149Arg
XM_011527546.2:c.446T>G	XP_011525848.1:p.Leu149Arg
NM_001302961.2:c.161T>G	NP_001289890.1:p.Leu54Arg
NR_126566.2:n.439T>G
NM_004917.5:c.446T>G MANE Select	NP_004908.4:p.Leu149Arg