Canonical Allele Identifier: CA508313872
Gene: KLK4 HGNC NCBI

Linked Data

dbSNP Id: rs2090455082
MyVariant Identifiers: chr19:g.51411844G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50908588G>A , CM000681.2:g.50908588G>A GRCh38
NC_000019.9:g.51411844G>A , CM000681.1:g.51411844G>A GRCh37
NC_000019.8:g.56103656G>A NCBI36
NG_012154.2:g.7151C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000324041.6:c.466C>T MANE Select ENSP00000326159.1:p.Leu156=
ENST00000324041.5:c.466C>T ENSP00000326159.1:p.Leu156=
ENST00000431178.2:c.319C>T ENSP00000399448.2:p.Leu107=
ENST00000593885.1:c.181C>T ENSP00000469769.1:p.Leu61=
ENST00000596876.1:n.385C>T
ENST00000598305.5:c.181C>T ENSP00000469963.1:p.Leu61=
ENST00000599865.5:n.319C>T
ENST00000602148.1:c.478C>T ENSP00000472091.1:n.478C>T
NM_001302961.1:c.181C>T NP_001289890.1:p.Leu61=
NM_004917.4:c.466C>T NP_004908.4:p.Leu156=
NR_126566.1:n.459C>T
XM_005259441.3:c.181C>T XP_005259498.2:p.Leu61=
XM_011527545.1:c.466C>T XP_011525847.1:p.Leu156=
XM_011527546.1:c.466C>T XP_011525848.1:p.Leu156=
XM_011527547.1:c.319C>T XP_011525849.1:p.Leu107=
XM_005259441.4:c.181C>T XP_005259498.2:p.Leu61=
XM_011527545.3:c.466C>T XP_011525847.1:p.Leu156=
XM_011527546.2:c.466C>T XP_011525848.1:p.Leu156=
NM_001302961.2:c.181C>T NP_001289890.1:p.Leu61=
NR_126566.2:n.459C>T
NM_004917.5:c.466C>T MANE Select NP_004908.4:p.Leu156=