Canonical Allele Identifier: CA2586648186
Gene: KLK4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50908316A>T , CM000681.2:g.50908316A>T GRCh38
NC_000019.9:g.51411572A>T , CM000681.1:g.51411572A>T GRCh37
NC_000019.8:g.56103384A>T NCBI36
NG_012154.2:g.7423T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000324041.6:c.612+43T>A MANE Select ENSP00000326159.1:n.612+43T>A
ENST00000324041.5:c.612+43T>A ENSP00000326159.1:n.612+43T>A
ENST00000431178.2:c.328+263T>A ENSP00000399448.2:n.328+263T>A
ENST00000593885.1:c.*107+43T>A ENSP00000469769.1:n.*107+43T>A
ENST00000596876.1:n.657T>A
ENST00000598305.5:c.*107+43T>A ENSP00000469963.1:n.*107+43T>A
ENST00000599865.5:n.548+43T>A
ENST00000602148.1:c.624+43T>A ENSP00000472091.1:n.624+43T>A
NM_001302961.1:c.327+43T>A NP_001289890.1:n.327+43T>A
NM_004917.4:c.612+43T>A NP_004908.4:n.612+43T>A
NR_126566.1:n.601+43T>A
XM_005259441.3:c.327+43T>A XP_005259498.2:n.327+43T>A
XM_011527546.1:c.475+263T>A XP_011525848.1:n.475+263T>A
XM_011527547.1:c.465+43T>A XP_011525849.1:n.465+43T>A
XM_005259441.4:c.327+43T>A XP_005259498.2:n.327+43T>A
XM_011527546.2:c.475+263T>A XP_011525848.1:n.475+263T>A
NM_001302961.2:c.327+43T>A NP_001289890.1:n.327+43T>A
NR_126566.2:n.601+43T>A
NM_004917.5:c.612+43T>A MANE Select NP_004908.4:n.612+43T>A