Canonical Allele Identifier: CA9605049
Gene: KLK4 HGNC NCBI

Linked Data

dbSNP Id: rs771848170

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50908524dup , CM000681.2:g.50908524dup GRCh38
NC_000019.9:g.51411780dup , CM000681.1:g.51411780dup GRCh37
NC_000019.8:g.56103592dup NCBI36
NG_012154.2:g.7219dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000324041.6:c.476-25dup MANE Select ENSP00000326159.1:n.476-25dup
ENST00000324041.5:c.476-25dup ENSP00000326159.1:n.476-25dup
ENST00000431178.2:c.328+59dup ENSP00000399448.2:n.328+59dup
ENST00000593885.1:c.191-29dup ENSP00000469769.1:n.191-29dup
ENST00000596876.1:n.453dup
ENST00000598305.5:c.191-29dup ENSP00000469963.1:n.191-29dup
ENST00000599865.5:n.387dup
ENST00000602148.1:c.488-25dup ENSP00000472091.1:n.488-25dup
NM_001302961.1:c.191-25dup NP_001289890.1:n.191-25dup
NM_004917.4:c.476-25dup NP_004908.4:n.476-25dup
NR_126566.1:n.469-29dup
XM_005259441.3:c.191-25dup XP_005259498.2:n.191-25dup
XM_011527545.1:c.476-29dup XP_011525847.1:n.476-29dup
XM_011527546.1:c.475+59dup XP_011525848.1:n.475+59dup
XM_011527547.1:c.329-25dup XP_011525849.1:n.329-25dup
XM_005259441.4:c.191-25dup XP_005259498.2:n.191-25dup
XM_011527545.3:c.476-29dup XP_011525847.1:n.476-29dup
XM_011527546.2:c.475+59dup XP_011525848.1:n.475+59dup
NM_001302961.2:c.191-25dup NP_001289890.1:n.191-25dup
NR_126566.2:n.469-29dup
NM_004917.5:c.476-25dup MANE Select NP_004908.4:n.476-25dup