Canonical Allele Identifier: CA407040603
Gene: KLK4 HGNC NCBI

Linked Data

dbSNP Id: rs2090452967

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50908422G>C , CM000681.2:g.50908422G>C GRCh38
NC_000019.9:g.51411678G>C , CM000681.1:g.51411678G>C GRCh37
NC_000019.8:g.56103490G>C NCBI36
NG_012154.2:g.7317C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000324041.6:c.549C>G MANE Select ENSP00000326159.1:p.Asp183Glu
ENST00000324041.5:c.549C>G ENSP00000326159.1:p.Asp183Glu
ENST00000431178.2:c.328+157C>G ENSP00000399448.2:n.328+157C>G
ENST00000593885.1:c.*44C>G ENSP00000469769.1:n.*44C>G
ENST00000596876.1:n.551C>G
ENST00000598305.5:c.*44C>G ENSP00000469963.1:n.*44C>G
ENST00000599865.5:n.485C>G
ENST00000602148.1:c.561C>G ENSP00000472091.1:n.561C>G
NM_001302961.1:c.264C>G NP_001289890.1:p.Asp88Glu
NM_004917.4:c.549C>G NP_004908.4:p.Asp183Glu
NR_126566.1:n.538C>G
XM_005259441.3:c.264C>G XP_005259498.2:p.Asp88Glu
XM_011527545.1:c.*44C>G XP_011525847.1:n.*44C>G
XM_011527546.1:c.475+157C>G XP_011525848.1:n.475+157C>G
XM_011527547.1:c.402C>G XP_011525849.1:p.Asp134Glu
XM_005259441.4:c.264C>G XP_005259498.2:p.Asp88Glu
XM_011527545.3:c.*44C>G XP_011525847.1:n.*44C>G
XM_011527546.2:c.475+157C>G XP_011525848.1:n.475+157C>G
NM_001302961.2:c.264C>G NP_001289890.1:p.Asp88Glu
NR_126566.2:n.538C>G
NM_004917.5:c.549C>G MANE Select NP_004908.4:p.Asp183Glu