Canonical Allele Identifier: CA508313848
Gene: KLK4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.51412016C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50908760C>T , CM000681.2:g.50908760C>T GRCh38
NC_000019.9:g.51412016C>T , CM000681.1:g.51412016C>T GRCh37
NC_000019.8:g.56103828C>T NCBI36
NG_012154.2:g.6979G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000324041.6:c.294G>A MANE Select ENSP00000326159.1:p.Glu98=
ENST00000324041.5:c.294G>A ENSP00000326159.1:p.Glu98=
ENST00000431178.2:c.147G>A ENSP00000399448.2:p.Glu49=
ENST00000593885.1:c.9G>A ENSP00000469769.1:p.Glu3=
ENST00000596876.1:n.213G>A
ENST00000598305.5:c.9G>A ENSP00000469963.1:p.Glu3=
ENST00000599865.5:n.147G>A
ENST00000602148.1:c.306G>A ENSP00000472091.1:n.306G>A
NM_001302961.1:c.9G>A NP_001289890.1:p.Glu3=
NM_004917.4:c.294G>A NP_004908.4:p.Glu98=
NR_126566.1:n.287G>A
XM_005259441.3:c.9G>A XP_005259498.2:p.Glu3=
XM_011527545.1:c.294G>A XP_011525847.1:p.Glu98=
XM_011527546.1:c.294G>A XP_011525848.1:p.Glu98=
XM_011527547.1:c.147G>A XP_011525849.1:p.Glu49=
XM_005259441.4:c.9G>A XP_005259498.2:p.Glu3=
XM_011527545.3:c.294G>A XP_011525847.1:p.Glu98=
XM_011527546.2:c.294G>A XP_011525848.1:p.Glu98=
NM_001302961.2:c.9G>A NP_001289890.1:p.Glu3=
NR_126566.2:n.287G>A
NM_004917.5:c.294G>A MANE Select NP_004908.4:p.Glu98=