Canonical Allele Identifier: CA407041407

Gene: KLK4

Linked Data

• MyVariant Identifiers: chr19:g.51411882G>T (hg19) ; chr19:g.50908626G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908626G>T , CM000681.2:g.50908626G>T	GRCh38
NC_000019.9:g.51411882G>T , CM000681.1:g.51411882G>T	GRCh37
NC_000019.8:g.56103694G>T	NCBI36
NG_012154.2:g.7113C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.428C>A MANE Select	ENSP00000326159.1:p.Thr143Asn
ENST00000324041.5:c.428C>A	ENSP00000326159.1:p.Thr143Asn
ENST00000431178.2:c.281C>A	ENSP00000399448.2:p.Thr94Asn
ENST00000593885.1:c.143C>A	ENSP00000469769.1:p.Thr48Asn
ENST00000596876.1:n.347C>A
ENST00000598305.5:c.143C>A	ENSP00000469963.1:p.Thr48Asn
ENST00000599865.5:n.281C>A
ENST00000602148.1:c.440C>A	ENSP00000472091.1:n.440C>A
NM_001302961.1:c.143C>A	NP_001289890.1:p.Thr48Asn
NM_004917.4:c.428C>A	NP_004908.4:p.Thr143Asn
NR_126566.1:n.421C>A
XM_005259441.3:c.143C>A	XP_005259498.2:p.Thr48Asn
XM_011527545.1:c.428C>A	XP_011525847.1:p.Thr143Asn
XM_011527546.1:c.428C>A	XP_011525848.1:p.Thr143Asn
XM_011527547.1:c.281C>A	XP_011525849.1:p.Thr94Asn
XM_005259441.4:c.143C>A	XP_005259498.2:p.Thr48Asn
XM_011527545.3:c.428C>A	XP_011525847.1:p.Thr143Asn
XM_011527546.2:c.428C>A	XP_011525848.1:p.Thr143Asn
NM_001302961.2:c.143C>A	NP_001289890.1:p.Thr48Asn
NR_126566.2:n.421C>A
NM_004917.5:c.428C>A MANE Select	NP_004908.4:p.Thr143Asn