Canonical Allele Identifier: CA9605036

Gene: KLK4

Linked Data

• dbSNP Id: rs755047973
• ExAC: 19:51411711 C / T
• gnomAD v2: 19-51411711-C-T
• MyVariant Identifiers: chr19:g.51411711C>T (hg19) ; chr19:g.50908455C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908455C>T , CM000681.2:g.50908455C>T	GRCh38
NC_000019.9:g.51411711C>T , CM000681.1:g.51411711C>T	GRCh37
NC_000019.8:g.56103523C>T	NCBI36
NG_012154.2:g.7284G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.516G>A MANE Select	ENSP00000326159.1:p.Val172=
ENST00000324041.5:c.516G>A	ENSP00000326159.1:p.Val172=
ENST00000431178.2:c.328+124G>A	ENSP00000399448.2:n.328+124G>A
ENST00000593885.1:c.*11G>A	ENSP00000469769.1:n.*11G>A
ENST00000596876.1:n.518G>A
ENST00000598305.5:c.*11G>A	ENSP00000469963.1:n.*11G>A
ENST00000599865.5:n.452G>A
ENST00000602148.1:c.528G>A	ENSP00000472091.1:n.528G>A
NM_001302961.1:c.231G>A	NP_001289890.1:p.Val77=
NM_004917.4:c.516G>A	NP_004908.4:p.Val172=
NR_126566.1:n.505G>A
XM_005259441.3:c.231G>A	XP_005259498.2:p.Val77=
XM_011527545.1:c.*11G>A	XP_011525847.1:n.*11G>A
XM_011527546.1:c.475+124G>A	XP_011525848.1:n.475+124G>A
XM_011527547.1:c.369G>A	XP_011525849.1:p.Val123=
XM_005259441.4:c.231G>A	XP_005259498.2:p.Val77=
XM_011527545.3:c.*11G>A	XP_011525847.1:n.*11G>A
XM_011527546.2:c.475+124G>A	XP_011525848.1:n.475+124G>A
NM_001302961.2:c.231G>A	NP_001289890.1:p.Val77=
NR_126566.2:n.505G>A
NM_004917.5:c.516G>A MANE Select	NP_004908.4:p.Val172=