Canonical Allele Identifier: CA407040639

Gene: KLK4

Linked Data

• MyVariant Identifiers: chr19:g.51411685A>C (hg19) ; chr19:g.50908429A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908429A>C , CM000681.2:g.50908429A>C	GRCh38
NC_000019.9:g.51411685A>C , CM000681.1:g.51411685A>C	GRCh37
NC_000019.8:g.56103497A>C	NCBI36
NG_012154.2:g.7310T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.542T>G MANE Select	ENSP00000326159.1:p.Leu181Arg
ENST00000324041.5:c.542T>G	ENSP00000326159.1:p.Leu181Arg
ENST00000431178.2:c.328+150T>G	ENSP00000399448.2:n.328+150T>G
ENST00000593885.1:c.*37T>G	ENSP00000469769.1:n.*37T>G
ENST00000596876.1:n.544T>G
ENST00000598305.5:c.*37T>G	ENSP00000469963.1:n.*37T>G
ENST00000599865.5:n.478T>G
ENST00000602148.1:c.554T>G	ENSP00000472091.1:n.554T>G
NM_001302961.1:c.257T>G	NP_001289890.1:p.Leu86Arg
NM_004917.4:c.542T>G	NP_004908.4:p.Leu181Arg
NR_126566.1:n.531T>G
XM_005259441.3:c.257T>G	XP_005259498.2:p.Leu86Arg
XM_011527545.1:c.*37T>G	XP_011525847.1:n.*37T>G
XM_011527546.1:c.475+150T>G	XP_011525848.1:n.475+150T>G
XM_011527547.1:c.395T>G	XP_011525849.1:p.Leu132Arg
XM_005259441.4:c.257T>G	XP_005259498.2:p.Leu86Arg
XM_011527545.3:c.*37T>G	XP_011525847.1:n.*37T>G
XM_011527546.2:c.475+150T>G	XP_011525848.1:n.475+150T>G
NM_001302961.2:c.257T>G	NP_001289890.1:p.Leu86Arg
NR_126566.2:n.531T>G
NM_004917.5:c.542T>G MANE Select	NP_004908.4:p.Leu181Arg