Canonical Allele Identifier: CA9605104

Gene: KLK4

Linked Data

• dbSNP Id: rs751557027
• ExAC: 19:51412033 C / A
• gnomAD v2: 19-51412033-C-A
• gnomAD v4: 19-50908777-C-A
• MyVariant Identifiers: chr19:g.51412033C>A (hg19) ; chr19:g.50908777C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908777C>A , CM000681.2:g.50908777C>A	GRCh38
NC_000019.9:g.51412033C>A , CM000681.1:g.51412033C>A	GRCh37
NC_000019.8:g.56103845C>A	NCBI36
NG_012154.2:g.6962G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.277G>T MANE Select	ENSP00000326159.1:p.Gly93Trp
ENST00000324041.5:c.277G>T	ENSP00000326159.1:p.Gly93Trp
ENST00000431178.2:c.130G>T	ENSP00000399448.2:p.Gly44Trp
ENST00000593885.1:c.-9G>T	ENSP00000469769.1:n.-9G>T
ENST00000596876.1:n.196G>T
ENST00000598305.5:c.-9G>T	ENSP00000469963.1:n.-9G>T
ENST00000599865.5:n.130G>T
ENST00000602148.1:c.289G>T	ENSP00000472091.1:n.289G>T
NM_001302961.1:c.-9G>T	NP_001289890.1:n.-9G>T
NM_004917.4:c.277G>T	NP_004908.4:p.Gly93Trp
NR_126566.1:n.270G>T
XM_005259441.3:c.-9G>T	XP_005259498.2:n.-9G>T
XM_011527545.1:c.277G>T	XP_011525847.1:p.Gly93Trp
XM_011527546.1:c.277G>T	XP_011525848.1:p.Gly93Trp
XM_011527547.1:c.130G>T	XP_011525849.1:p.Gly44Trp
XM_005259441.4:c.-9G>T	XP_005259498.2:n.-9G>T
XM_011527545.3:c.277G>T	XP_011525847.1:p.Gly93Trp
XM_011527546.2:c.277G>T	XP_011525848.1:p.Gly93Trp
NM_001302961.2:c.-9G>T	NP_001289890.1:n.-9G>T
NR_126566.2:n.270G>T
NM_004917.5:c.277G>T MANE Select	NP_004908.4:p.Gly93Trp