Canonical Allele Identifier: CA633710635

Gene: KLK4

Linked Data

• dbSNP Id: rs1429714836
• gnomAD v2: 19-51411354-G-T
• gnomAD v3: 19-50908098-G-T
• gnomAD v4: 19-50908098-G-T
• MyVariant Identifiers: chr19:g.51411354G>T (hg19) ; chr19:g.50908098G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908098G>T , CM000681.2:g.50908098G>T	GRCh38
NC_000019.9:g.51411354G>T , CM000681.1:g.51411354G>T	GRCh37
NC_000019.8:g.56103166G>T	NCBI36
NG_012154.2:g.7641C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.612+261C>A MANE Select	ENSP00000326159.1:n.612+261C>A
ENST00000324041.5:c.612+261C>A	ENSP00000326159.1:n.612+261C>A
ENST00000431178.2:c.328+481C>A	ENSP00000399448.2:n.328+481C>A
ENST00000593885.1:c.*107+261C>A	ENSP00000469769.1:n.*107+261C>A
ENST00000596876.1:n.875C>A
ENST00000598305.5:c.*107+261C>A	ENSP00000469963.1:n.*107+261C>A
ENST00000599865.5:n.548+261C>A
ENST00000602148.1:c.624+261C>A	ENSP00000472091.1:n.624+261C>A
NM_001302961.1:c.327+261C>A	NP_001289890.1:n.327+261C>A
NM_004917.4:c.612+261C>A	NP_004908.4:n.612+261C>A
NR_126566.1:n.601+261C>A
XM_005259441.3:c.327+261C>A	XP_005259498.2:n.327+261C>A
XM_011527546.1:c.475+481C>A	XP_011525848.1:n.475+481C>A
XM_011527547.1:c.465+261C>A	XP_011525849.1:n.465+261C>A
XM_005259441.4:c.327+261C>A	XP_005259498.2:n.327+261C>A
XM_011527546.2:c.475+481C>A	XP_011525848.1:n.475+481C>A
NM_001302961.2:c.327+261C>A	NP_001289890.1:n.327+261C>A
NR_126566.2:n.601+261C>A
NM_004917.5:c.612+261C>A MANE Select	NP_004908.4:n.612+261C>A