Canonical Allele Identifier: CA407040812

Gene: KLK4

Linked Data

• gnomAD v4: 19-50908457-C-A
• MyVariant Identifiers: chr19:g.51411713C>A (hg19) ; chr19:g.50908457C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908457C>A , CM000681.2:g.50908457C>A	GRCh38
NC_000019.9:g.51411713C>A , CM000681.1:g.51411713C>A	GRCh37
NC_000019.8:g.56103525C>A	NCBI36
NG_012154.2:g.7282G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.514G>T MANE Select	ENSP00000326159.1:p.Val172Leu
ENST00000324041.5:c.514G>T	ENSP00000326159.1:p.Val172Leu
ENST00000431178.2:c.328+122G>T	ENSP00000399448.2:n.328+122G>T
ENST00000593885.1:c.*9G>T	ENSP00000469769.1:n.*9G>T
ENST00000596876.1:n.516G>T
ENST00000598305.5:c.*9G>T	ENSP00000469963.1:n.*9G>T
ENST00000599865.5:n.450G>T
ENST00000602148.1:c.526G>T	ENSP00000472091.1:n.526G>T
NM_001302961.1:c.229G>T	NP_001289890.1:p.Val77Leu
NM_004917.4:c.514G>T	NP_004908.4:p.Val172Leu
NR_126566.1:n.503G>T
XM_005259441.3:c.229G>T	XP_005259498.2:p.Val77Leu
XM_011527545.1:c.*9G>T	XP_011525847.1:n.*9G>T
XM_011527546.1:c.475+122G>T	XP_011525848.1:n.475+122G>T
XM_011527547.1:c.367G>T	XP_011525849.1:p.Val123Leu
XM_005259441.4:c.229G>T	XP_005259498.2:p.Val77Leu
XM_011527545.3:c.*9G>T	XP_011525847.1:n.*9G>T
XM_011527546.2:c.475+122G>T	XP_011525848.1:n.475+122G>T
NM_001302961.2:c.229G>T	NP_001289890.1:p.Val77Leu
NR_126566.2:n.503G>T
NM_004917.5:c.514G>T MANE Select	NP_004908.4:p.Val172Leu