Canonical Allele Identifier: CA407040761

Gene: KLK4

Linked Data

• MyVariant Identifiers: chr19:g.51411701C>A (hg19) ; chr19:g.50908445C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908445C>A , CM000681.2:g.50908445C>A	GRCh38
NC_000019.9:g.51411701C>A , CM000681.1:g.51411701C>A	GRCh37
NC_000019.8:g.56103513C>A	NCBI36
NG_012154.2:g.7294G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.526G>T MANE Select	ENSP00000326159.1:p.Glu176Ter
ENST00000324041.5:c.526G>T	ENSP00000326159.1:p.Glu176Ter
ENST00000431178.2:c.328+134G>T	ENSP00000399448.2:n.328+134G>T
ENST00000593885.1:c.*21G>T	ENSP00000469769.1:n.*21G>T
ENST00000596876.1:n.528G>T
ENST00000598305.5:c.*21G>T	ENSP00000469963.1:n.*21G>T
ENST00000599865.5:n.462G>T
ENST00000602148.1:c.538G>T	ENSP00000472091.1:n.538G>T
NM_001302961.1:c.241G>T	NP_001289890.1:p.Glu81Ter
NM_004917.4:c.526G>T	NP_004908.4:p.Glu176Ter
NR_126566.1:n.515G>T
XM_005259441.3:c.241G>T	XP_005259498.2:p.Glu81Ter
XM_011527545.1:c.*21G>T	XP_011525847.1:n.*21G>T
XM_011527546.1:c.475+134G>T	XP_011525848.1:n.475+134G>T
XM_011527547.1:c.379G>T	XP_011525849.1:p.Glu127Ter
XM_005259441.4:c.241G>T	XP_005259498.2:p.Glu81Ter
XM_011527545.3:c.*21G>T	XP_011525847.1:n.*21G>T
XM_011527546.2:c.475+134G>T	XP_011525848.1:n.475+134G>T
NM_001302961.2:c.241G>T	NP_001289890.1:p.Glu81Ter
NR_126566.2:n.515G>T
NM_004917.5:c.526G>T MANE Select	NP_004908.4:p.Glu176Ter