Canonical Allele Identifier: CA309674386

Gene: KLK8

Linked Data

• dbSNP Id: rs975911963
• gnomAD v3: 19-50997030-G-A
• gnomAD v4: 19-50997030-G-A
• MyVariant Identifiers: chr19:g.51500286G>A (hg19) ; chr19:g.50997030G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50997030G>A , CM000681.2:g.50997030G>A	GRCh38
NC_000019.9:g.51500286G>A , CM000681.1:g.51500286G>A	GRCh37
NC_000019.8:g.56192098G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000695909.1:c.627+721C>T MANE Select	ENSP00000512260.1:n.627+721C>T
ENST00000291726.11:c.264+721C>T	ENSP00000291726.8:n.264+721C>T
ENST00000320838.9:c.71-816C>T	ENSP00000325072.5:n.71-816C>T
ENST00000347619.8:c.204+721C>T	ENSP00000341555.3:n.204+721C>T
ENST00000391806.6:c.762+721C>T	ENSP00000375682.1:n.762+721C>T
ENST00000593490.1:c.71-816C>T	ENSP00000469278.1:n.71-816C>T
ENST00000594669.1:c.426+721C>T
ENST00000594914.1:n.217+721C>T
ENST00000598195.5:n.417+721C>T
ENST00000599166.5:c.1191+721C>T	ENSP00000471395.1:n.1191+721C>T
ENST00000600767.5:c.627+721C>T	ENSP00000472016.1:n.627+721C>T
NM_001281431.1:c.264+721C>T	NP_001268360.1:n.264+721C>T
NM_007196.3:c.627+721C>T	NP_009127.1:n.627+721C>T
NM_144505.2:c.762+721C>T	NP_653088.1:n.762+721C>T
NM_144506.2:c.204+721C>T	NP_653089.1:n.204+721C>T
NM_144507.2:c.71-816C>T	NP_653090.1:n.71-816C>T
NR_104008.1:n.543+721C>T
NM_007196.4:c.627+721C>T MANE Select	NP_009127.1:n.627+721C>T
NM_144505.3:c.762+721C>T	NP_653088.1:n.762+721C>T
NM_144506.3:c.204+721C>T	NP_653089.1:n.204+721C>T
NR_104008.2:n.445+721C>T
NM_001281431.2:c.264+721C>T	NP_001268360.1:n.264+721C>T
NM_144507.3:c.71-816C>T	NP_653090.1:n.71-816C>T