Canonical Allele Identifier: CA633899560

Gene: KLK4

Linked Data

• dbSNP Id: rs373865620
• gnomAD v2: 19-51411780-C-T
• gnomAD v3: 19-50908524-C-T
• gnomAD v4: 19-50908524-C-T
• COSMIC: COSN20045691
• MyVariant Identifiers: chr19:g.51411780C>T (hg19) ; chr19:g.50908524C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908524C>T , CM000681.2:g.50908524C>T	GRCh38
NC_000019.9:g.51411780C>T , CM000681.1:g.51411780C>T	GRCh37
NC_000019.8:g.56103592C>T	NCBI36
NG_012154.2:g.7215G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000324041.6:c.476-29G>A MANE Select	ENSP00000326159.1:n.476-29G>A
ENST00000324041.5:c.476-29G>A	ENSP00000326159.1:n.476-29G>A
ENST00000431178.2:c.328+55G>A	ENSP00000399448.2:n.328+55G>A
ENST00000593885.1:c.191-33G>A	ENSP00000469769.1:n.191-33G>A
ENST00000596876.1:n.449G>A
ENST00000598305.5:c.191-33G>A	ENSP00000469963.1:n.191-33G>A
ENST00000599865.5:n.383G>A
ENST00000602148.1:c.488-29G>A	ENSP00000472091.1:n.488-29G>A
NM_001302961.1:c.191-29G>A	NP_001289890.1:n.191-29G>A
NM_004917.4:c.476-29G>A	NP_004908.4:n.476-29G>A
NR_126566.1:n.469-33G>A
XM_005259441.3:c.191-29G>A	XP_005259498.2:n.191-29G>A
XM_011527545.1:c.476-33G>A	XP_011525847.1:n.476-33G>A
XM_011527546.1:c.475+55G>A	XP_011525848.1:n.475+55G>A
XM_011527547.1:c.329-29G>A	XP_011525849.1:n.329-29G>A
XM_005259441.4:c.191-29G>A	XP_005259498.2:n.191-29G>A
XM_011527545.3:c.476-33G>A	XP_011525847.1:n.476-33G>A
XM_011527546.2:c.475+55G>A	XP_011525848.1:n.475+55G>A
NM_001302961.2:c.191-29G>A	NP_001289890.1:n.191-29G>A
NR_126566.2:n.469-33G>A
NM_004917.5:c.476-29G>A MANE Select	NP_004908.4:n.476-29G>A