Canonical Allele Identifier: CA2586648142

Gene: KLK4

Linked Data

• gnomAD v4: 19-50908251-CTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908257_50908258del , CM000681.2:g.50908257_50908258del	GRCh38
NC_000019.9:g.51411513_51411514del , CM000681.1:g.51411513_51411514del	GRCh37
NC_000019.8:g.56103325_56103326del	NCBI36
NG_012154.2:g.7486_7487del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.612+106_612+107del MANE Select	ENSP00000326159.1:n.612+106_612+107del
ENST00000324041.5:c.612+106_612+107del	ENSP00000326159.1:n.612+106_612+107del
ENST00000431178.2:c.328+326_328+327del	ENSP00000399448.2:n.328+326_328+327del
ENST00000593885.1:c.*107+106_*107+107del	ENSP00000469769.1:n.*107+106_*107+107del
ENST00000596876.1:n.720_721del
ENST00000598305.5:c.*107+106_*107+107del	ENSP00000469963.1:n.*107+106_*107+107del
ENST00000599865.5:n.548+106_548+107del
ENST00000602148.1:c.624+106_624+107del	ENSP00000472091.1:n.624+106_624+107del
NM_001302961.1:c.327+106_327+107del	NP_001289890.1:n.327+106_327+107del
NM_004917.4:c.612+106_612+107del	NP_004908.4:n.612+106_612+107del
NR_126566.1:n.601+106_601+107del
XM_005259441.3:c.327+106_327+107del	XP_005259498.2:n.327+106_327+107del
XM_011527546.1:c.475+326_475+327del	XP_011525848.1:n.475+326_475+327del
XM_011527547.1:c.465+106_465+107del	XP_011525849.1:n.465+106_465+107del
XM_005259441.4:c.327+106_327+107del	XP_005259498.2:n.327+106_327+107del
XM_011527546.2:c.475+326_475+327del	XP_011525848.1:n.475+326_475+327del
NM_001302961.2:c.327+106_327+107del	NP_001289890.1:n.327+106_327+107del
NR_126566.2:n.601+106_601+107del
NM_004917.5:c.612+106_612+107del MANE Select	NP_004908.4:n.612+106_612+107del