Canonical Allele Identifier: CA2341183418
Gene: KLK8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50996987A= , CM000681.2:g.50996987A= GRCh38
NC_000019.9:g.51500243A= , CM000681.1:g.51500243A= GRCh37
NC_000019.8:g.56192055A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000695909.1:c.627+764T= MANE Select ENSP00000512260.1:n.627+764T=
ENST00000291726.11:c.264+764T= ENSP00000291726.8:n.264+764T=
ENST00000320838.9:c.71-773T= ENSP00000325072.5:n.71-773T=
ENST00000347619.8:c.204+764T= ENSP00000341555.3:n.204+764T=
ENST00000391806.6:c.762+764T= ENSP00000375682.1:n.762+764T=
ENST00000593490.1:c.71-773T= ENSP00000469278.1:n.71-773T=
ENST00000594669.1:c.426+764T=
ENST00000594914.1:n.217+764T=
ENST00000598195.5:n.417+764T=
ENST00000599166.5:c.1191+764T= ENSP00000471395.1:n.1191+764T=
ENST00000600767.5:c.627+764T= ENSP00000472016.1:n.627+764T=
NM_001281431.1:c.264+764T= NP_001268360.1:n.264+764T=
NM_007196.3:c.627+764T= NP_009127.1:n.627+764T=
NM_144505.2:c.762+764T= NP_653088.1:n.762+764T=
NM_144506.2:c.204+764T= NP_653089.1:n.204+764T=
NM_144507.2:c.71-773T= NP_653090.1:n.71-773T=
NR_104008.1:n.543+764T=
NM_007196.4:c.627+764T= MANE Select NP_009127.1:n.627+764T=
NM_144505.3:c.762+764T= NP_653088.1:n.762+764T=
NM_144506.3:c.204+764T= NP_653089.1:n.204+764T=
NR_104008.2:n.445+764T=
NM_001281431.2:c.264+764T= NP_001268360.1:n.264+764T=
NM_144507.3:c.71-773T= NP_653090.1:n.71-773T=