Canonical Allele Identifier: CA309661918

Gene: KLK4

Linked Data

• dbSNP Id: rs1034027930
• gnomAD v3: 19-50908220-TCA-T
• gnomAD v4: 19-50908220-TCA-T
• MyVariant Identifiers: chr19:g.51411477_51411478del (hg19) ; chr19:g.50908221_50908222del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908221_50908222del , CM000681.2:g.50908221_50908222del	GRCh38
NC_000019.9:g.51411477_51411478del , CM000681.1:g.51411477_51411478del	GRCh37
NC_000019.8:g.56103289_56103290del	NCBI36
NG_012154.2:g.7517_7518del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.612+137_612+138del MANE Select	ENSP00000326159.1:n.612+137_612+138del
ENST00000324041.5:c.612+137_612+138del	ENSP00000326159.1:n.612+137_612+138del
ENST00000431178.2:c.328+357_328+358del	ENSP00000399448.2:n.328+357_328+358del
ENST00000593885.1:c.*107+137_*107+138del	ENSP00000469769.1:n.*107+137_*107+138del
ENST00000596876.1:n.751_752del
ENST00000598305.5:c.*107+137_*107+138del	ENSP00000469963.1:n.*107+137_*107+138del
ENST00000599865.5:n.548+137_548+138del
ENST00000602148.1:c.624+137_624+138del	ENSP00000472091.1:n.624+137_624+138del
NM_001302961.1:c.327+137_327+138del	NP_001289890.1:n.327+137_327+138del
NM_004917.4:c.612+137_612+138del	NP_004908.4:n.612+137_612+138del
NR_126566.1:n.601+137_601+138del
XM_005259441.3:c.327+137_327+138del	XP_005259498.2:n.327+137_327+138del
XM_011527546.1:c.475+357_475+358del	XP_011525848.1:n.475+357_475+358del
XM_011527547.1:c.465+137_465+138del	XP_011525849.1:n.465+137_465+138del
XM_005259441.4:c.327+137_327+138del	XP_005259498.2:n.327+137_327+138del
XM_011527546.2:c.475+357_475+358del	XP_011525848.1:n.475+357_475+358del
NM_001302961.2:c.327+137_327+138del	NP_001289890.1:n.327+137_327+138del
NR_126566.2:n.601+137_601+138del
NM_004917.5:c.612+137_612+138del MANE Select	NP_004908.4:n.612+137_612+138del