Canonical Allele Identifier: CA2341183426
Gene: KLK8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50997023C= , CM000681.2:g.50997023C= GRCh38
NC_000019.9:g.51500279C= , CM000681.1:g.51500279C= GRCh37
NC_000019.8:g.56192091C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000695909.1:c.627+728G= MANE Select ENSP00000512260.1:n.627+728G=
ENST00000291726.11:c.264+728G= ENSP00000291726.8:n.264+728G=
ENST00000320838.9:c.71-809G= ENSP00000325072.5:n.71-809G=
ENST00000347619.8:c.204+728G= ENSP00000341555.3:n.204+728G=
ENST00000391806.6:c.762+728G= ENSP00000375682.1:n.762+728G=
ENST00000593490.1:c.71-809G= ENSP00000469278.1:n.71-809G=
ENST00000594669.1:c.426+728G=
ENST00000594914.1:n.217+728G=
ENST00000598195.5:n.417+728G=
ENST00000599166.5:c.1191+728G= ENSP00000471395.1:n.1191+728G=
ENST00000600767.5:c.627+728G= ENSP00000472016.1:n.627+728G=
NM_001281431.1:c.264+728G= NP_001268360.1:n.264+728G=
NM_007196.3:c.627+728G= NP_009127.1:n.627+728G=
NM_144505.2:c.762+728G= NP_653088.1:n.762+728G=
NM_144506.2:c.204+728G= NP_653089.1:n.204+728G=
NM_144507.2:c.71-809G= NP_653090.1:n.71-809G=
NR_104008.1:n.543+728G=
NM_007196.4:c.627+728G= MANE Select NP_009127.1:n.627+728G=
NM_144505.3:c.762+728G= NP_653088.1:n.762+728G=
NM_144506.3:c.204+728G= NP_653089.1:n.204+728G=
NR_104008.2:n.445+728G=
NM_001281431.2:c.264+728G= NP_001268360.1:n.264+728G=
NM_144507.3:c.71-809G= NP_653090.1:n.71-809G=