Canonical Allele Identifier: CA883221856

Gene: KLK4

Linked Data

• dbSNP Id: rs1265526236
• gnomAD v4: 19-50908212-TGTTTCTCTCA-T
• MyVariant Identifiers: chr19:g.51411469_51411478del (hg19) ; chr19:g.50908213_50908222del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908222_50908231del , CM000681.2:g.50908222_50908231del	GRCh38
NC_000019.9:g.51411478_51411487del , CM000681.1:g.51411478_51411487del	GRCh37
NC_000019.8:g.56103290_56103299del	NCBI36
NG_012154.2:g.7517_7526del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.612+137_612+146del MANE Select	ENSP00000326159.1:n.612+137_612+146del
ENST00000324041.5:c.612+137_612+146del	ENSP00000326159.1:n.612+137_612+146del
ENST00000431178.2:c.328+357_328+366del	ENSP00000399448.2:n.328+357_328+366del
ENST00000593885.1:c.*107+137_*107+146del	ENSP00000469769.1:n.*107+137_*107+146del
ENST00000596876.1:n.751_760del
ENST00000598305.5:c.*107+137_*107+146del	ENSP00000469963.1:n.*107+137_*107+146del
ENST00000599865.5:n.548+137_548+146del
ENST00000602148.1:c.624+137_624+146del	ENSP00000472091.1:n.624+137_624+146del
NM_001302961.1:c.327+137_327+146del	NP_001289890.1:n.327+137_327+146del
NM_004917.4:c.612+137_612+146del	NP_004908.4:n.612+137_612+146del
NR_126566.1:n.601+137_601+146del
XM_005259441.3:c.327+137_327+146del	XP_005259498.2:n.327+137_327+146del
XM_011527546.1:c.475+357_475+366del	XP_011525848.1:n.475+357_475+366del
XM_011527547.1:c.465+137_465+146del	XP_011525849.1:n.465+137_465+146del
XM_005259441.4:c.327+137_327+146del	XP_005259498.2:n.327+137_327+146del
XM_011527546.2:c.475+357_475+366del	XP_011525848.1:n.475+357_475+366del
NM_001302961.2:c.327+137_327+146del	NP_001289890.1:n.327+137_327+146del
NR_126566.2:n.601+137_601+146del
NM_004917.5:c.612+137_612+146del MANE Select	NP_004908.4:n.612+137_612+146del