Canonical Allele Identifier: CA9605057

Gene: KLK4

Linked Data

• dbSNP Id: rs773051441
• ExAC: 19:51411809 GGGCAGA / G
• gnomAD v2: 19-51411809-GGGCAGA-G
• gnomAD v3: 19-50908553-GGGCAGA-G
• gnomAD v4: 19-50908553-GGGCAGA-G
• MyVariant Identifiers: chr19:g.51411810_51411815del (hg19) ; chr19:g.50908554_50908559del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908554_50908559del , CM000681.2:g.50908554_50908559del	GRCh38
NC_000019.9:g.51411810_51411815del , CM000681.1:g.51411810_51411815del	GRCh37
NC_000019.8:g.56103622_56103627del	NCBI36
NG_012154.2:g.7180_7185del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.475+20_475+25del MANE Select	ENSP00000326159.1:n.475+20_475+25del
ENST00000324041.5:c.475+20_475+25del	ENSP00000326159.1:n.475+20_475+25del
ENST00000431178.2:c.328+20_328+25del	ENSP00000399448.2:n.328+20_328+25del
ENST00000593885.1:c.190+20_190+25del	ENSP00000469769.1:n.190+20_190+25del
ENST00000596876.1:n.414_419del
ENST00000598305.5:c.190+20_190+25del	ENSP00000469963.1:n.190+20_190+25del
ENST00000599865.5:n.348_353del
ENST00000602148.1:c.487+20_487+25del	ENSP00000472091.1:n.487+20_487+25del
NM_001302961.1:c.190+20_190+25del	NP_001289890.1:n.190+20_190+25del
NM_004917.4:c.475+20_475+25del	NP_004908.4:n.475+20_475+25del
NR_126566.1:n.468+20_468+25del
XM_005259441.3:c.190+20_190+25del	XP_005259498.2:n.190+20_190+25del
XM_011527545.1:c.475+20_475+25del	XP_011525847.1:n.475+20_475+25del
XM_011527546.1:c.475+20_475+25del	XP_011525848.1:n.475+20_475+25del
XM_011527547.1:c.328+20_328+25del	XP_011525849.1:n.328+20_328+25del
XM_005259441.4:c.190+20_190+25del	XP_005259498.2:n.190+20_190+25del
XM_011527545.3:c.475+20_475+25del	XP_011525847.1:n.475+20_475+25del
XM_011527546.2:c.475+20_475+25del	XP_011525848.1:n.475+20_475+25del
NM_001302961.2:c.190+20_190+25del	NP_001289890.1:n.190+20_190+25del
NR_126566.2:n.468+20_468+25del
NM_004917.5:c.475+20_475+25del MANE Select	NP_004908.4:n.475+20_475+25del