Canonical Allele Identifier: CA996856546
Gene: KLK8 HGNC NCBI

Linked Data

dbSNP Id: rs2091174608

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50996902A>G , CM000681.2:g.50996902A>G GRCh38
NC_000019.9:g.51500158A>G , CM000681.1:g.51500158A>G GRCh37
NC_000019.8:g.56191970A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000695909.1:c.628-688T>C MANE Select ENSP00000512260.1:n.628-688T>C
ENST00000291726.11:c.265-688T>C ENSP00000291726.8:n.265-688T>C
ENST00000320838.9:c.71-688T>C ENSP00000325072.5:n.71-688T>C
ENST00000347619.8:c.205-688T>C ENSP00000341555.3:n.205-688T>C
ENST00000391806.6:c.763-688T>C ENSP00000375682.1:n.763-688T>C
ENST00000593490.1:c.71-688T>C ENSP00000469278.1:n.71-688T>C
ENST00000594669.1:c.427-688T>C
ENST00000594914.1:n.218-688T>C
ENST00000598195.5:n.418-688T>C
ENST00000599166.5:c.1192-688T>C ENSP00000471395.1:n.1192-688T>C
ENST00000600767.5:c.628-688T>C ENSP00000472016.1:n.628-688T>C
NM_001281431.1:c.265-688T>C NP_001268360.1:n.265-688T>C
NM_007196.3:c.628-688T>C NP_009127.1:n.628-688T>C
NM_144505.2:c.763-688T>C NP_653088.1:n.763-688T>C
NM_144506.2:c.205-688T>C NP_653089.1:n.205-688T>C
NM_144507.2:c.71-688T>C NP_653090.1:n.71-688T>C
NR_104008.1:n.544-688T>C
NM_007196.4:c.628-688T>C MANE Select NP_009127.1:n.628-688T>C
NM_144505.3:c.763-688T>C NP_653088.1:n.763-688T>C
NM_144506.3:c.205-688T>C NP_653089.1:n.205-688T>C
NR_104008.2:n.446-688T>C
NM_001281431.2:c.265-688T>C NP_001268360.1:n.265-688T>C
NM_144507.3:c.71-688T>C NP_653090.1:n.71-688T>C