Canonical Allele Identifier: CA633899561

Gene: KLK4

Linked Data

• dbSNP Id: rs542046361
• gnomAD v2: 19-51411781-G-A
• gnomAD v4: 19-50908525-G-A
• COSMIC: COSN20065966
• MyVariant Identifiers: chr19:g.51411781G>A (hg19) ; chr19:g.50908525G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908525G>A , CM000681.2:g.50908525G>A	GRCh38
NC_000019.9:g.51411781G>A , CM000681.1:g.51411781G>A	GRCh37
NC_000019.8:g.56103593G>A	NCBI36
NG_012154.2:g.7214C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000324041.6:c.476-30C>T MANE Select	ENSP00000326159.1:n.476-30C>T
ENST00000324041.5:c.476-30C>T	ENSP00000326159.1:n.476-30C>T
ENST00000431178.2:c.328+54C>T	ENSP00000399448.2:n.328+54C>T
ENST00000593885.1:c.191-34C>T	ENSP00000469769.1:n.191-34C>T
ENST00000596876.1:n.448C>T
ENST00000598305.5:c.191-34C>T	ENSP00000469963.1:n.191-34C>T
ENST00000599865.5:n.382C>T
ENST00000602148.1:c.488-30C>T	ENSP00000472091.1:n.488-30C>T
NM_001302961.1:c.191-30C>T	NP_001289890.1:n.191-30C>T
NM_004917.4:c.476-30C>T	NP_004908.4:n.476-30C>T
NR_126566.1:n.469-34C>T
XM_005259441.3:c.191-30C>T	XP_005259498.2:n.191-30C>T
XM_011527545.1:c.476-34C>T	XP_011525847.1:n.476-34C>T
XM_011527546.1:c.475+54C>T	XP_011525848.1:n.475+54C>T
XM_011527547.1:c.329-30C>T	XP_011525849.1:n.329-30C>T
XM_005259441.4:c.191-30C>T	XP_005259498.2:n.191-30C>T
XM_011527545.3:c.476-34C>T	XP_011525847.1:n.476-34C>T
XM_011527546.2:c.475+54C>T	XP_011525848.1:n.475+54C>T
NM_001302961.2:c.191-30C>T	NP_001289890.1:n.191-30C>T
NR_126566.2:n.469-34C>T
NM_004917.5:c.476-30C>T MANE Select	NP_004908.4:n.476-30C>T