Canonical Allele Identifier: CA2341138349
Gene: KLK4 HGNC NCBI

Linked Data

dbSNP Id: rs1454432442

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50908568C>T , CM000681.2:g.50908568C>T GRCh38
NC_000019.9:g.51411824C>T , CM000681.1:g.51411824C>T GRCh37
NC_000019.8:g.56103636C>T NCBI36
NG_012154.2:g.7171G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000324041.6:c.475+11G>A MANE Select ENSP00000326159.1:n.475+11G>A
ENST00000324041.5:c.475+11G>A ENSP00000326159.1:n.475+11G>A
ENST00000431178.2:c.328+11G>A ENSP00000399448.2:n.328+11G>A
ENST00000593885.1:c.190+11G>A ENSP00000469769.1:n.190+11G>A
ENST00000596876.1:n.405G>A
ENST00000598305.5:c.190+11G>A ENSP00000469963.1:n.190+11G>A
ENST00000599865.5:n.339G>A
ENST00000602148.1:c.487+11G>A ENSP00000472091.1:n.487+11G>A
NM_001302961.1:c.190+11G>A NP_001289890.1:n.190+11G>A
NM_004917.4:c.475+11G>A NP_004908.4:n.475+11G>A
NR_126566.1:n.468+11G>A
XM_005259441.3:c.190+11G>A XP_005259498.2:n.190+11G>A
XM_011527545.1:c.475+11G>A XP_011525847.1:n.475+11G>A
XM_011527546.1:c.475+11G>A XP_011525848.1:n.475+11G>A
XM_011527547.1:c.328+11G>A XP_011525849.1:n.328+11G>A
XM_005259441.4:c.190+11G>A XP_005259498.2:n.190+11G>A
XM_011527545.3:c.475+11G>A XP_011525847.1:n.475+11G>A
XM_011527546.2:c.475+11G>A XP_011525848.1:n.475+11G>A
NM_001302961.2:c.190+11G>A NP_001289890.1:n.190+11G>A
NR_126566.2:n.468+11G>A
NM_004917.5:c.475+11G>A MANE Select NP_004908.4:n.475+11G>A