Canonical Allele Identifier: CA407041622

Gene: KLK4

Linked Data

• MyVariant Identifiers: chr19:g.51411964C>G (hg19) ; chr19:g.50908708C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908708C>G , CM000681.2:g.50908708C>G	GRCh38
NC_000019.9:g.51411964C>G , CM000681.1:g.51411964C>G	GRCh37
NC_000019.8:g.56103776C>G	NCBI36
NG_012154.2:g.7031G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.346G>C MANE Select	ENSP00000326159.1:p.Asp116His
ENST00000324041.5:c.346G>C	ENSP00000326159.1:p.Asp116His
ENST00000431178.2:c.199G>C	ENSP00000399448.2:p.Asp67His
ENST00000593885.1:c.61G>C	ENSP00000469769.1:p.Asp21His
ENST00000596876.1:n.265G>C
ENST00000598305.5:c.61G>C	ENSP00000469963.1:p.Asp21His
ENST00000599865.5:n.199G>C
ENST00000602148.1:c.358G>C	ENSP00000472091.1:n.358G>C
NM_001302961.1:c.61G>C	NP_001289890.1:p.Asp21His
NM_004917.4:c.346G>C	NP_004908.4:p.Asp116His
NR_126566.1:n.339G>C
XM_005259441.3:c.61G>C	XP_005259498.2:p.Asp21His
XM_011527545.1:c.346G>C	XP_011525847.1:p.Asp116His
XM_011527546.1:c.346G>C	XP_011525848.1:p.Asp116His
XM_011527547.1:c.199G>C	XP_011525849.1:p.Asp67His
XM_005259441.4:c.61G>C	XP_005259498.2:p.Asp21His
XM_011527545.3:c.346G>C	XP_011525847.1:p.Asp116His
XM_011527546.2:c.346G>C	XP_011525848.1:p.Asp116His
NM_001302961.2:c.61G>C	NP_001289890.1:p.Asp21His
NR_126566.2:n.339G>C
NM_004917.5:c.346G>C MANE Select	NP_004908.4:p.Asp116His