Canonical Allele Identifier: CA2843048092

Gene: KLK8

Genomic Alleles

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

Transcript Alleles

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