Canonical Allele Identifier: CA2586648087

Gene: KLK4

Linked Data

• gnomAD v4: 19-50908190-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908190T>C , CM000681.2:g.50908190T>C	GRCh38
NC_000019.9:g.51411446T>C , CM000681.1:g.51411446T>C	GRCh37
NC_000019.8:g.56103258T>C	NCBI36
NG_012154.2:g.7549A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.612+169A>G MANE Select	ENSP00000326159.1:n.612+169A>G
ENST00000324041.5:c.612+169A>G	ENSP00000326159.1:n.612+169A>G
ENST00000431178.2:c.328+389A>G	ENSP00000399448.2:n.328+389A>G
ENST00000593885.1:c.*107+169A>G	ENSP00000469769.1:n.*107+169A>G
ENST00000596876.1:n.783A>G
ENST00000598305.5:c.*107+169A>G	ENSP00000469963.1:n.*107+169A>G
ENST00000599865.5:n.548+169A>G
ENST00000602148.1:c.624+169A>G	ENSP00000472091.1:n.624+169A>G
NM_001302961.1:c.327+169A>G	NP_001289890.1:n.327+169A>G
NM_004917.4:c.612+169A>G	NP_004908.4:n.612+169A>G
NR_126566.1:n.601+169A>G
XM_005259441.3:c.327+169A>G	XP_005259498.2:n.327+169A>G
XM_011527546.1:c.475+389A>G	XP_011525848.1:n.475+389A>G
XM_011527547.1:c.465+169A>G	XP_011525849.1:n.465+169A>G
XM_005259441.4:c.327+169A>G	XP_005259498.2:n.327+169A>G
XM_011527546.2:c.475+389A>G	XP_011525848.1:n.475+389A>G
NM_001302961.2:c.327+169A>G	NP_001289890.1:n.327+169A>G
NR_126566.2:n.601+169A>G
NM_004917.5:c.612+169A>G MANE Select	NP_004908.4:n.612+169A>G