Canonical Allele Identifier: CA633899556

Gene: KLK4

Linked Data

• dbSNP Id: rs771848170
• gnomAD v2: 19-51411775-GC-G
• gnomAD v4: 19-50908519-GC-G
• MyVariant Identifiers: chr19:g.51411776del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908524del , CM000681.2:g.50908524del	GRCh38
NC_000019.9:g.51411780del , CM000681.1:g.51411780del	GRCh37
NC_000019.8:g.56103592del	NCBI36
NG_012154.2:g.7219del

Transcript Alleles

HGVS	Amino-acid change
ENST00000324041.6:c.476-25del MANE Select	ENSP00000326159.1:n.476-25del
ENST00000324041.5:c.476-25del	ENSP00000326159.1:n.476-25del
ENST00000431178.2:c.328+59del	ENSP00000399448.2:n.328+59del
ENST00000593885.1:c.191-29del	ENSP00000469769.1:n.191-29del
ENST00000596876.1:n.453del
ENST00000598305.5:c.191-29del	ENSP00000469963.1:n.191-29del
ENST00000599865.5:n.387del
ENST00000602148.1:c.488-25del	ENSP00000472091.1:n.488-25del
NM_001302961.1:c.191-25del	NP_001289890.1:n.191-25del
NM_004917.4:c.476-25del	NP_004908.4:n.476-25del
NR_126566.1:n.469-29del
XM_005259441.3:c.191-25del	XP_005259498.2:n.191-25del
XM_011527545.1:c.476-29del	XP_011525847.1:n.476-29del
XM_011527546.1:c.475+59del	XP_011525848.1:n.475+59del
XM_011527547.1:c.329-25del	XP_011525849.1:n.329-25del
XM_005259441.4:c.191-25del	XP_005259498.2:n.191-25del
XM_011527545.3:c.476-29del	XP_011525847.1:n.476-29del
XM_011527546.2:c.475+59del	XP_011525848.1:n.475+59del
NM_001302961.2:c.191-25del	NP_001289890.1:n.191-25del
NR_126566.2:n.469-29del
NM_004917.5:c.476-25del MANE Select	NP_004908.4:n.476-25del