Canonical Allele Identifier: CA9605071
Gene: KLK4 HGNC NCBI

Linked Data

dbSNP Id: rs530069905

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50908624C>A , CM000681.2:g.50908624C>A GRCh38
NC_000019.9:g.51411880C>A , CM000681.1:g.51411880C>A GRCh37
NC_000019.8:g.56103692C>A NCBI36
NG_012154.2:g.7115G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000324041.6:c.430G>T MANE Select ENSP00000326159.1:p.Ala144Ser
ENST00000324041.5:c.430G>T ENSP00000326159.1:p.Ala144Ser
ENST00000431178.2:c.283G>T ENSP00000399448.2:p.Ala95Ser
ENST00000593885.1:c.145G>T ENSP00000469769.1:p.Ala49Ser
ENST00000596876.1:n.349G>T
ENST00000598305.5:c.145G>T ENSP00000469963.1:p.Ala49Ser
ENST00000599865.5:n.283G>T
ENST00000602148.1:c.442G>T ENSP00000472091.1:n.442G>T
NM_001302961.1:c.145G>T NP_001289890.1:p.Ala49Ser
NM_004917.4:c.430G>T NP_004908.4:p.Ala144Ser
NR_126566.1:n.423G>T
XM_005259441.3:c.145G>T XP_005259498.2:p.Ala49Ser
XM_011527545.1:c.430G>T XP_011525847.1:p.Ala144Ser
XM_011527546.1:c.430G>T XP_011525848.1:p.Ala144Ser
XM_011527547.1:c.283G>T XP_011525849.1:p.Ala95Ser
XM_005259441.4:c.145G>T XP_005259498.2:p.Ala49Ser
XM_011527545.3:c.430G>T XP_011525847.1:p.Ala144Ser
XM_011527546.2:c.430G>T XP_011525848.1:p.Ala144Ser
NM_001302961.2:c.145G>T NP_001289890.1:p.Ala49Ser
NR_126566.2:n.423G>T
NM_004917.5:c.430G>T MANE Select NP_004908.4:p.Ala144Ser