Canonical Allele Identifier: CA508313966
Gene: KLK4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.51411938T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50908682T>C , CM000681.2:g.50908682T>C GRCh38
NC_000019.9:g.51411938T>C , CM000681.1:g.51411938T>C GRCh37
NC_000019.8:g.56103750T>C NCBI36
NG_012154.2:g.7057A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000324041.6:c.372A>G MANE Select ENSP00000326159.1:p.Glu124=
ENST00000324041.5:c.372A>G ENSP00000326159.1:p.Glu124=
ENST00000431178.2:c.225A>G ENSP00000399448.2:p.Glu75=
ENST00000593885.1:c.87A>G ENSP00000469769.1:p.Glu29=
ENST00000596876.1:n.291A>G
ENST00000598305.5:c.87A>G ENSP00000469963.1:p.Glu29=
ENST00000599865.5:n.225A>G
ENST00000602148.1:c.384A>G ENSP00000472091.1:n.384A>G
NM_001302961.1:c.87A>G NP_001289890.1:p.Glu29=
NM_004917.4:c.372A>G NP_004908.4:p.Glu124=
NR_126566.1:n.365A>G
XM_005259441.3:c.87A>G XP_005259498.2:p.Glu29=
XM_011527545.1:c.372A>G XP_011525847.1:p.Glu124=
XM_011527546.1:c.372A>G XP_011525848.1:p.Glu124=
XM_011527547.1:c.225A>G XP_011525849.1:p.Glu75=
XM_005259441.4:c.87A>G XP_005259498.2:p.Glu29=
XM_011527545.3:c.372A>G XP_011525847.1:p.Glu124=
XM_011527546.2:c.372A>G XP_011525848.1:p.Glu124=
NM_001302961.2:c.87A>G NP_001289890.1:p.Glu29=
NR_126566.2:n.365A>G
NM_004917.5:c.372A>G MANE Select NP_004908.4:p.Glu124=