Canonical Allele Identifier: CA2586648208
Gene: KLK4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50908535A>T , CM000681.2:g.50908535A>T GRCh38
NC_000019.9:g.51411791A>T , CM000681.1:g.51411791A>T GRCh37
NC_000019.8:g.56103603A>T NCBI36
NG_012154.2:g.7204T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000324041.6:c.476-40T>A MANE Select ENSP00000326159.1:n.476-40T>A
ENST00000324041.5:c.476-40T>A ENSP00000326159.1:n.476-40T>A
ENST00000431178.2:c.328+44T>A ENSP00000399448.2:n.328+44T>A
ENST00000593885.1:c.191-44T>A ENSP00000469769.1:n.191-44T>A
ENST00000596876.1:n.438T>A
ENST00000598305.5:c.191-44T>A ENSP00000469963.1:n.191-44T>A
ENST00000599865.5:n.372T>A
ENST00000602148.1:c.488-40T>A ENSP00000472091.1:n.488-40T>A
NM_001302961.1:c.191-40T>A NP_001289890.1:n.191-40T>A
NM_004917.4:c.476-40T>A NP_004908.4:n.476-40T>A
NR_126566.1:n.469-44T>A
XM_005259441.3:c.191-40T>A XP_005259498.2:n.191-40T>A
XM_011527545.1:c.476-44T>A XP_011525847.1:n.476-44T>A
XM_011527546.1:c.475+44T>A XP_011525848.1:n.475+44T>A
XM_011527547.1:c.329-40T>A XP_011525849.1:n.329-40T>A
XM_005259441.4:c.191-40T>A XP_005259498.2:n.191-40T>A
XM_011527545.3:c.476-44T>A XP_011525847.1:n.476-44T>A
XM_011527546.2:c.475+44T>A XP_011525848.1:n.475+44T>A
NM_001302961.2:c.191-40T>A NP_001289890.1:n.191-40T>A
NR_126566.2:n.469-44T>A
NM_004917.5:c.476-40T>A MANE Select NP_004908.4:n.476-40T>A