Canonical Allele Identifier: CA2341138362
Gene: KLK4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50908601_50908602delinsAG , CM000681.2:g.50908601_50908602delinsAG GRCh38
NC_000019.9:g.51411857_51411858delinsAG , CM000681.1:g.51411857_51411858delinsAG GRCh37
NC_000019.8:g.56103669_56103670delinsAG NCBI36
NG_012154.2:g.7137_7138delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000324041.6:c.452_453delinsCT MANE Select ENSP00000326159.1:p.Ser151=
ENST00000324041.5:c.452_453delinsCT ENSP00000326159.1:p.Ser151=
ENST00000431178.2:c.305_306delinsCT ENSP00000399448.2:p.Ser102=
ENST00000593885.1:c.167_168delinsCT ENSP00000469769.1:p.Ser56=
ENST00000596876.1:n.371_372delinsCT
ENST00000598305.5:c.167_168delinsCT ENSP00000469963.1:p.Ser56=
ENST00000599865.5:n.305_306delinsCT
ENST00000602148.1:c.464_465delinsCT ENSP00000472091.1:n.464_465delinsCT
NM_001302961.1:c.167_168delinsCT NP_001289890.1:p.Ser56=
NM_004917.4:c.452_453delinsCT NP_004908.4:p.Ser151=
NR_126566.1:n.445_446delinsCT
XM_005259441.3:c.167_168delinsCT XP_005259498.2:p.Ser56=
XM_011527545.1:c.452_453delinsCT XP_011525847.1:p.Ser151=
XM_011527546.1:c.452_453delinsCT XP_011525848.1:p.Ser151=
XM_011527547.1:c.305_306delinsCT XP_011525849.1:p.Ser102=
XM_005259441.4:c.167_168delinsCT XP_005259498.2:p.Ser56=
XM_011527545.3:c.452_453delinsCT XP_011525847.1:p.Ser151=
XM_011527546.2:c.452_453delinsCT XP_011525848.1:p.Ser151=
NM_001302961.2:c.167_168delinsCT NP_001289890.1:p.Ser56=
NR_126566.2:n.445_446delinsCT
NM_004917.5:c.452_453delinsCT MANE Select NP_004908.4:p.Ser151=