Canonical Allele Identifier: CA2586648163

Gene: KLK4

Linked Data

• gnomAD v4: 19-50908280-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908280C>A , CM000681.2:g.50908280C>A	GRCh38
NC_000019.9:g.51411536C>A , CM000681.1:g.51411536C>A	GRCh37
NC_000019.8:g.56103348C>A	NCBI36
NG_012154.2:g.7459G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.612+79G>T MANE Select	ENSP00000326159.1:n.612+79G>T
ENST00000324041.5:c.612+79G>T	ENSP00000326159.1:n.612+79G>T
ENST00000431178.2:c.328+299G>T	ENSP00000399448.2:n.328+299G>T
ENST00000593885.1:c.*107+79G>T	ENSP00000469769.1:n.*107+79G>T
ENST00000596876.1:n.693G>T
ENST00000598305.5:c.*107+79G>T	ENSP00000469963.1:n.*107+79G>T
ENST00000599865.5:n.548+79G>T
ENST00000602148.1:c.624+79G>T	ENSP00000472091.1:n.624+79G>T
NM_001302961.1:c.327+79G>T	NP_001289890.1:n.327+79G>T
NM_004917.4:c.612+79G>T	NP_004908.4:n.612+79G>T
NR_126566.1:n.601+79G>T
XM_005259441.3:c.327+79G>T	XP_005259498.2:n.327+79G>T
XM_011527546.1:c.475+299G>T	XP_011525848.1:n.475+299G>T
XM_011527547.1:c.465+79G>T	XP_011525849.1:n.465+79G>T
XM_005259441.4:c.327+79G>T	XP_005259498.2:n.327+79G>T
XM_011527546.2:c.475+299G>T	XP_011525848.1:n.475+299G>T
NM_001302961.2:c.327+79G>T	NP_001289890.1:n.327+79G>T
NR_126566.2:n.601+79G>T
NM_004917.5:c.612+79G>T MANE Select	NP_004908.4:n.612+79G>T