Canonical Allele Identifier: CA508211920

Gene: KLK4

Linked Data

• MyVariant Identifiers: chr19:g.51411674G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908418G>A , CM000681.2:g.50908418G>A	GRCh38
NC_000019.9:g.51411674G>A , CM000681.1:g.51411674G>A	GRCh37
NC_000019.8:g.56103486G>A	NCBI36
NG_012154.2:g.7321C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.553C>T MANE Select	ENSP00000326159.1:p.Leu185=
ENST00000324041.5:c.553C>T	ENSP00000326159.1:p.Leu185=
ENST00000431178.2:c.328+161C>T	ENSP00000399448.2:n.328+161C>T
ENST00000593885.1:c.*48C>T	ENSP00000469769.1:n.*48C>T
ENST00000596876.1:n.555C>T
ENST00000598305.5:c.*48C>T	ENSP00000469963.1:n.*48C>T
ENST00000599865.5:n.489C>T
ENST00000602148.1:c.565C>T	ENSP00000472091.1:n.565C>T
NM_001302961.1:c.268C>T	NP_001289890.1:p.Leu90=
NM_004917.4:c.553C>T	NP_004908.4:p.Leu185=
NR_126566.1:n.542C>T
XM_005259441.3:c.268C>T	XP_005259498.2:p.Leu90=
XM_011527545.1:c.*48C>T	XP_011525847.1:n.*48C>T
XM_011527546.1:c.475+161C>T	XP_011525848.1:n.475+161C>T
XM_011527547.1:c.406C>T	XP_011525849.1:p.Leu136=
XM_005259441.4:c.268C>T	XP_005259498.2:p.Leu90=
XM_011527545.3:c.*48C>T	XP_011525847.1:n.*48C>T
XM_011527546.2:c.475+161C>T	XP_011525848.1:n.475+161C>T
NM_001302961.2:c.268C>T	NP_001289890.1:p.Leu90=
NR_126566.2:n.542C>T
NM_004917.5:c.553C>T MANE Select	NP_004908.4:p.Leu185=