Canonical Allele Identifier: CA2586648110

Gene: KLK4

Linked Data

• gnomAD v4: 19-50908215-TTCTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908218_50908221del , CM000681.2:g.50908218_50908221del	GRCh38
NC_000019.9:g.51411474_51411477del , CM000681.1:g.51411474_51411477del	GRCh37
NC_000019.8:g.56103286_56103289del	NCBI36
NG_012154.2:g.7520_7523del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.612+140_612+143del MANE Select	ENSP00000326159.1:n.612+140_612+143del
ENST00000324041.5:c.612+140_612+143del	ENSP00000326159.1:n.612+140_612+143del
ENST00000431178.2:c.328+360_328+363del	ENSP00000399448.2:n.328+360_328+363del
ENST00000593885.1:c.*107+140_*107+143del	ENSP00000469769.1:n.*107+140_*107+143del
ENST00000596876.1:n.754_757del
ENST00000598305.5:c.*107+140_*107+143del	ENSP00000469963.1:n.*107+140_*107+143del
ENST00000599865.5:n.548+140_548+143del
ENST00000602148.1:c.624+140_624+143del	ENSP00000472091.1:n.624+140_624+143del
NM_001302961.1:c.327+140_327+143del	NP_001289890.1:n.327+140_327+143del
NM_004917.4:c.612+140_612+143del	NP_004908.4:n.612+140_612+143del
NR_126566.1:n.601+140_601+143del
XM_005259441.3:c.327+140_327+143del	XP_005259498.2:n.327+140_327+143del
XM_011527546.1:c.475+360_475+363del	XP_011525848.1:n.475+360_475+363del
XM_011527547.1:c.465+140_465+143del	XP_011525849.1:n.465+140_465+143del
XM_005259441.4:c.327+140_327+143del	XP_005259498.2:n.327+140_327+143del
XM_011527546.2:c.475+360_475+363del	XP_011525848.1:n.475+360_475+363del
NM_001302961.2:c.327+140_327+143del	NP_001289890.1:n.327+140_327+143del
NR_126566.2:n.601+140_601+143del
NM_004917.5:c.612+140_612+143del MANE Select	NP_004908.4:n.612+140_612+143del