Canonical Allele Identifier: CA407040351

Gene: KLK4

Linked Data

• MyVariant Identifiers: chr19:g.50908380T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908380T>A , CM000681.2:g.50908380T>A	GRCh38
NG_012154.2:g.7359A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.591A>T MANE Select	ENSP00000326159.1:p.Gln197His
ENST00000324041.5:c.591A>T	ENSP00000326159.1:p.Gln197His
ENST00000431178.2:c.328+199A>T	ENSP00000399448.2:n.328+199A>T
ENST00000593885.1:c.*86A>T	ENSP00000469769.1:n.*86A>T
ENST00000596876.1:n.593A>T
ENST00000598305.5:c.*86A>T	ENSP00000469963.1:n.*86A>T
ENST00000599865.5:n.527A>T
ENST00000602148.1:c.603A>T	ENSP00000472091.1:n.603A>T
NM_001302961.1:c.306A>T	NP_001289890.1:p.Gln102His
NM_004917.4:c.591A>T	NP_004908.4:p.Gln197His
NR_126566.1:n.580A>T
XM_005259441.3:c.306A>T	XP_005259498.2:p.Gln102His
XM_011527546.1:c.475+199A>T	XP_011525848.1:n.475+199A>T
XM_011527547.1:c.444A>T	XP_011525849.1:p.Gln148His
XM_005259441.4:c.306A>T	XP_005259498.2:p.Gln102His
XM_011527545.3:c.*86A>T	XP_011525847.1:n.*86A>T
XM_011527546.2:c.475+199A>T	XP_011525848.1:n.475+199A>T
NM_001302961.2:c.306A>T	NP_001289890.1:p.Gln102His
NR_126566.2:n.580A>T
NM_004917.5:c.591A>T MANE Select	NP_004908.4:p.Gln197His