Canonical Allele Identifier: CA309661890

Gene: KLK4

Linked Data

• dbSNP Id: rs759235527
• gnomAD v3: 19-50908131-ATG-A
• gnomAD v4: 19-50908131-ATG-A
• MyVariant Identifiers: chr19:g.51411388_51411389del (hg19) ; chr19:g.50908132_50908133del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908141_50908142del , CM000681.2:g.50908141_50908142del	GRCh38
NC_000019.9:g.51411397_51411398del , CM000681.1:g.51411397_51411398del	GRCh37
NC_000019.8:g.56103209_56103210del	NCBI36
NG_012154.2:g.7606_7607del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.612+226_612+227del MANE Select	ENSP00000326159.1:n.612+226_612+227del
ENST00000324041.5:c.612+226_612+227del	ENSP00000326159.1:n.612+226_612+227del
ENST00000431178.2:c.328+446_328+447del	ENSP00000399448.2:n.328+446_328+447del
ENST00000593885.1:c.*107+226_*107+227del	ENSP00000469769.1:n.*107+226_*107+227del
ENST00000596876.1:n.840_841del
ENST00000598305.5:c.*107+226_*107+227del	ENSP00000469963.1:n.*107+226_*107+227del
ENST00000599865.5:n.548+226_548+227del
ENST00000602148.1:c.624+226_624+227del	ENSP00000472091.1:n.624+226_624+227del
NM_001302961.1:c.327+226_327+227del	NP_001289890.1:n.327+226_327+227del
NM_004917.4:c.612+226_612+227del	NP_004908.4:n.612+226_612+227del
NR_126566.1:n.601+226_601+227del
XM_005259441.3:c.327+226_327+227del	XP_005259498.2:n.327+226_327+227del
XM_011527546.1:c.475+446_475+447del	XP_011525848.1:n.475+446_475+447del
XM_011527547.1:c.465+226_465+227del	XP_011525849.1:n.465+226_465+227del
XM_005259441.4:c.327+226_327+227del	XP_005259498.2:n.327+226_327+227del
XM_011527546.2:c.475+446_475+447del	XP_011525848.1:n.475+446_475+447del
NM_001302961.2:c.327+226_327+227del	NP_001289890.1:n.327+226_327+227del
NR_126566.2:n.601+226_601+227del
NM_004917.5:c.612+226_612+227del MANE Select	NP_004908.4:n.612+226_612+227del