Canonical Allele Identifier: CA407041863
Gene: KLK4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50908824T>C , CM000681.2:g.50908824T>C GRCh38
NC_000019.9:g.51412080T>C , CM000681.1:g.51412080T>C GRCh37
NC_000019.8:g.56103892T>C NCBI36
NG_012154.2:g.6915A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000324041.6:c.230A>G MANE Select ENSP00000326159.1:p.Tyr77Cys
ENST00000324041.5:c.230A>G ENSP00000326159.1:p.Tyr77Cys
ENST00000431178.2:c.83A>G ENSP00000399448.2:p.Tyr28Cys
ENST00000593885.1:c.-56A>G ENSP00000469769.1:n.-56A>G
ENST00000596876.1:n.149A>G
ENST00000598305.5:c.-56A>G ENSP00000469963.1:n.-56A>G
ENST00000599865.5:n.83A>G
ENST00000602148.1:c.242A>G ENSP00000472091.1:n.242A>G
NM_001302961.1:c.-56A>G NP_001289890.1:n.-56A>G
NM_004917.4:c.230A>G NP_004908.4:p.Tyr77Cys
NR_126566.1:n.223A>G
XM_005259441.3:c.-56A>G XP_005259498.2:n.-56A>G
XM_011527545.1:c.230A>G XP_011525847.1:p.Tyr77Cys
XM_011527546.1:c.230A>G XP_011525848.1:p.Tyr77Cys
XM_011527547.1:c.83A>G XP_011525849.1:p.Tyr28Cys
XM_005259441.4:c.-56A>G XP_005259498.2:n.-56A>G
XM_011527545.3:c.230A>G XP_011525847.1:p.Tyr77Cys
XM_011527546.2:c.230A>G XP_011525848.1:p.Tyr77Cys
NM_001302961.2:c.-56A>G NP_001289890.1:n.-56A>G
NR_126566.2:n.223A>G
NM_004917.5:c.230A>G MANE Select NP_004908.4:p.Tyr77Cys