Canonical Allele Identifier: CA2586648202

Gene: KLK4

Linked Data

• gnomAD v4: 19-50908518-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908518A>C , CM000681.2:g.50908518A>C	GRCh38
NC_000019.9:g.51411774A>C , CM000681.1:g.51411774A>C	GRCh37
NC_000019.8:g.56103586A>C	NCBI36
NG_012154.2:g.7221T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000324041.6:c.476-23T>G MANE Select	ENSP00000326159.1:n.476-23T>G
ENST00000324041.5:c.476-23T>G	ENSP00000326159.1:n.476-23T>G
ENST00000431178.2:c.328+61T>G	ENSP00000399448.2:n.328+61T>G
ENST00000593885.1:c.191-27T>G	ENSP00000469769.1:n.191-27T>G
ENST00000596876.1:n.455T>G
ENST00000598305.5:c.191-27T>G	ENSP00000469963.1:n.191-27T>G
ENST00000599865.5:n.389T>G
ENST00000602148.1:c.488-23T>G	ENSP00000472091.1:n.488-23T>G
NM_001302961.1:c.191-23T>G	NP_001289890.1:n.191-23T>G
NM_004917.4:c.476-23T>G	NP_004908.4:n.476-23T>G
NR_126566.1:n.469-27T>G
XM_005259441.3:c.191-23T>G	XP_005259498.2:n.191-23T>G
XM_011527545.1:c.476-27T>G	XP_011525847.1:n.476-27T>G
XM_011527546.1:c.475+61T>G	XP_011525848.1:n.475+61T>G
XM_011527547.1:c.329-23T>G	XP_011525849.1:n.329-23T>G
XM_005259441.4:c.191-23T>G	XP_005259498.2:n.191-23T>G
XM_011527545.3:c.476-27T>G	XP_011525847.1:n.476-27T>G
XM_011527546.2:c.475+61T>G	XP_011525848.1:n.475+61T>G
NM_001302961.2:c.191-23T>G	NP_001289890.1:n.191-23T>G
NR_126566.2:n.469-27T>G
NM_004917.5:c.476-23T>G MANE Select	NP_004908.4:n.476-23T>G