Canonical Allele Identifier: CA407041521

Gene: KLK4

Linked Data

• MyVariant Identifiers: chr19:g.51411918G>A (hg19) ; chr19:g.50908662G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908662G>A , CM000681.2:g.50908662G>A	GRCh38
NC_000019.9:g.51411918G>A , CM000681.1:g.51411918G>A	GRCh37
NC_000019.8:g.56103730G>A	NCBI36
NG_012154.2:g.7077C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.392C>T MANE Select	ENSP00000326159.1:p.Thr131Ile
ENST00000324041.5:c.392C>T	ENSP00000326159.1:p.Thr131Ile
ENST00000431178.2:c.245C>T	ENSP00000399448.2:p.Thr82Ile
ENST00000593885.1:c.107C>T	ENSP00000469769.1:p.Thr36Ile
ENST00000596876.1:n.311C>T
ENST00000598305.5:c.107C>T	ENSP00000469963.1:p.Thr36Ile
ENST00000599865.5:n.245C>T
ENST00000602148.1:c.404C>T	ENSP00000472091.1:n.404C>T
NM_001302961.1:c.107C>T	NP_001289890.1:p.Thr36Ile
NM_004917.4:c.392C>T	NP_004908.4:p.Thr131Ile
NR_126566.1:n.385C>T
XM_005259441.3:c.107C>T	XP_005259498.2:p.Thr36Ile
XM_011527545.1:c.392C>T	XP_011525847.1:p.Thr131Ile
XM_011527546.1:c.392C>T	XP_011525848.1:p.Thr131Ile
XM_011527547.1:c.245C>T	XP_011525849.1:p.Thr82Ile
XM_005259441.4:c.107C>T	XP_005259498.2:p.Thr36Ile
XM_011527545.3:c.392C>T	XP_011525847.1:p.Thr131Ile
XM_011527546.2:c.392C>T	XP_011525848.1:p.Thr131Ile
NM_001302961.2:c.107C>T	NP_001289890.1:p.Thr36Ile
NR_126566.2:n.385C>T
NM_004917.5:c.392C>T MANE Select	NP_004908.4:p.Thr131Ile