Canonical Allele Identifier: CA633899555
Gene: KLK4 HGNC NCBI

Linked Data

dbSNP Id: rs1391403736

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50908518A>T , CM000681.2:g.50908518A>T GRCh38
NC_000019.9:g.51411774A>T , CM000681.1:g.51411774A>T GRCh37
NC_000019.8:g.56103586A>T NCBI36
NG_012154.2:g.7221T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000324041.6:c.476-23T>A MANE Select ENSP00000326159.1:n.476-23T>A
ENST00000324041.5:c.476-23T>A ENSP00000326159.1:n.476-23T>A
ENST00000431178.2:c.328+61T>A ENSP00000399448.2:n.328+61T>A
ENST00000593885.1:c.191-27T>A ENSP00000469769.1:n.191-27T>A
ENST00000596876.1:n.455T>A
ENST00000598305.5:c.191-27T>A ENSP00000469963.1:n.191-27T>A
ENST00000599865.5:n.389T>A
ENST00000602148.1:c.488-23T>A ENSP00000472091.1:n.488-23T>A
NM_001302961.1:c.191-23T>A NP_001289890.1:n.191-23T>A
NM_004917.4:c.476-23T>A NP_004908.4:n.476-23T>A
NR_126566.1:n.469-27T>A
XM_005259441.3:c.191-23T>A XP_005259498.2:n.191-23T>A
XM_011527545.1:c.476-27T>A XP_011525847.1:n.476-27T>A
XM_011527546.1:c.475+61T>A XP_011525848.1:n.475+61T>A
XM_011527547.1:c.329-23T>A XP_011525849.1:n.329-23T>A
XM_005259441.4:c.191-23T>A XP_005259498.2:n.191-23T>A
XM_011527545.3:c.476-27T>A XP_011525847.1:n.476-27T>A
XM_011527546.2:c.475+61T>A XP_011525848.1:n.475+61T>A
NM_001302961.2:c.191-23T>A NP_001289890.1:n.191-23T>A
NR_126566.2:n.469-27T>A
NM_004917.5:c.476-23T>A MANE Select NP_004908.4:n.476-23T>A