Canonical Allele Identifier: CA407041132

Gene: KLK4

Linked Data

• dbSNP Id: rs2090453681
• gnomAD v3: 19-50908475-G-A
• gnomAD v4: 19-50908475-G-A
• MyVariant Identifiers: chr19:g.51411731G>A (hg19) ; chr19:g.50908475G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908475G>A , CM000681.2:g.50908475G>A	GRCh38
NC_000019.9:g.51411731G>A , CM000681.1:g.51411731G>A	GRCh37
NC_000019.8:g.56103543G>A	NCBI36
NG_012154.2:g.7264C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.496C>T MANE Select	ENSP00000326159.1:p.Gln166Ter
ENST00000324041.5:c.496C>T	ENSP00000326159.1:p.Gln166Ter
ENST00000431178.2:c.328+104C>T	ENSP00000399448.2:n.328+104C>T
ENST00000593885.1:c.207C>T	ENSP00000469769.1:p.Cys69=
ENST00000596876.1:n.498C>T
ENST00000598305.5:c.207C>T	ENSP00000469963.1:p.Cys69=
ENST00000599865.5:n.432C>T
ENST00000602148.1:c.508C>T	ENSP00000472091.1:n.508C>T
NM_001302961.1:c.211C>T	NP_001289890.1:p.Gln71Ter
NM_004917.4:c.496C>T	NP_004908.4:p.Gln166Ter
NR_126566.1:n.485C>T
XM_005259441.3:c.211C>T	XP_005259498.2:p.Gln71Ter
XM_011527545.1:c.492C>T	XP_011525847.1:p.Cys164=
XM_011527546.1:c.475+104C>T	XP_011525848.1:n.475+104C>T
XM_011527547.1:c.349C>T	XP_011525849.1:p.Gln117Ter
XM_005259441.4:c.211C>T	XP_005259498.2:p.Gln71Ter
XM_011527545.3:c.492C>T	XP_011525847.1:p.Cys164=
XM_011527546.2:c.475+104C>T	XP_011525848.1:n.475+104C>T
NM_001302961.2:c.211C>T	NP_001289890.1:p.Gln71Ter
NR_126566.2:n.485C>T
NM_004917.5:c.496C>T MANE Select	NP_004908.4:p.Gln166Ter