Canonical Allele Identifier: CA996838577
Gene: KLK4 HGNC NCBI

Linked Data

dbSNP Id: rs2090449790

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50908131A>G , CM000681.2:g.50908131A>G GRCh38
NC_000019.9:g.51411387A>G , CM000681.1:g.51411387A>G GRCh37
NC_000019.8:g.56103199A>G NCBI36
NG_012154.2:g.7608T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000324041.6:c.612+228T>C MANE Select ENSP00000326159.1:n.612+228T>C
ENST00000324041.5:c.612+228T>C ENSP00000326159.1:n.612+228T>C
ENST00000431178.2:c.328+448T>C ENSP00000399448.2:n.328+448T>C
ENST00000593885.1:c.*107+228T>C ENSP00000469769.1:n.*107+228T>C
ENST00000596876.1:n.842T>C
ENST00000598305.5:c.*107+228T>C ENSP00000469963.1:n.*107+228T>C
ENST00000599865.5:n.548+228T>C
ENST00000602148.1:c.624+228T>C ENSP00000472091.1:n.624+228T>C
NM_001302961.1:c.327+228T>C NP_001289890.1:n.327+228T>C
NM_004917.4:c.612+228T>C NP_004908.4:n.612+228T>C
NR_126566.1:n.601+228T>C
XM_005259441.3:c.327+228T>C XP_005259498.2:n.327+228T>C
XM_011527546.1:c.475+448T>C XP_011525848.1:n.475+448T>C
XM_011527547.1:c.465+228T>C XP_011525849.1:n.465+228T>C
XM_005259441.4:c.327+228T>C XP_005259498.2:n.327+228T>C
XM_011527546.2:c.475+448T>C XP_011525848.1:n.475+448T>C
NM_001302961.2:c.327+228T>C NP_001289890.1:n.327+228T>C
NR_126566.2:n.601+228T>C
NM_004917.5:c.612+228T>C MANE Select NP_004908.4:n.612+228T>C