Canonical Allele Identifier: CA9605027
Gene: KLK4 HGNC NCBI

Linked Data

dbSNP Id: rs767315231

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50908407G>T , CM000681.2:g.50908407G>T GRCh38
NC_000019.9:g.51411663G>T , CM000681.1:g.51411663G>T GRCh37
NC_000019.8:g.56103475G>T NCBI36
NG_012154.2:g.7332C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000324041.6:c.564C>A MANE Select ENSP00000326159.1:p.Pro188=
ENST00000324041.5:c.564C>A ENSP00000326159.1:p.Pro188=
ENST00000431178.2:c.328+172C>A ENSP00000399448.2:n.328+172C>A
ENST00000593885.1:c.*59C>A ENSP00000469769.1:n.*59C>A
ENST00000596876.1:n.566C>A
ENST00000598305.5:c.*59C>A ENSP00000469963.1:n.*59C>A
ENST00000599865.5:n.500C>A
ENST00000602148.1:c.576C>A ENSP00000472091.1:n.576C>A
NM_001302961.1:c.279C>A NP_001289890.1:p.Pro93=
NM_004917.4:c.564C>A NP_004908.4:p.Pro188=
NR_126566.1:n.553C>A
XM_005259441.3:c.279C>A XP_005259498.2:p.Pro93=
XM_011527545.1:c.*59C>A XP_011525847.1:n.*59C>A
XM_011527546.1:c.475+172C>A XP_011525848.1:n.475+172C>A
XM_011527547.1:c.417C>A XP_011525849.1:p.Pro139=
XM_005259441.4:c.279C>A XP_005259498.2:p.Pro93=
XM_011527545.3:c.*59C>A XP_011525847.1:n.*59C>A
XM_011527546.2:c.475+172C>A XP_011525848.1:n.475+172C>A
NM_001302961.2:c.279C>A NP_001289890.1:p.Pro93=
NR_126566.2:n.553C>A
NM_004917.5:c.564C>A MANE Select NP_004908.4:p.Pro188=