Canonical Allele Identifier: CA407041129
Gene: KLK4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50908474T>C , CM000681.2:g.50908474T>C GRCh38
NC_000019.9:g.51411730T>C , CM000681.1:g.51411730T>C GRCh37
NC_000019.8:g.56103542T>C NCBI36
NG_012154.2:g.7265A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000324041.6:c.497A>G MANE Select ENSP00000326159.1:p.Gln166Arg
ENST00000324041.5:c.497A>G ENSP00000326159.1:p.Gln166Arg
ENST00000431178.2:c.328+105A>G ENSP00000399448.2:n.328+105A>G
ENST00000593885.1:c.208A>G ENSP00000469769.1:p.Ser70Gly
ENST00000596876.1:n.499A>G
ENST00000598305.5:c.208A>G ENSP00000469963.1:p.Ser70Gly
ENST00000599865.5:n.433A>G
ENST00000602148.1:c.509A>G ENSP00000472091.1:n.509A>G
NM_001302961.1:c.212A>G NP_001289890.1:p.Gln71Arg
NM_004917.4:c.497A>G NP_004908.4:p.Gln166Arg
NR_126566.1:n.486A>G
XM_005259441.3:c.212A>G XP_005259498.2:p.Gln71Arg
XM_011527545.1:c.493A>G XP_011525847.1:p.Ser165Gly
XM_011527546.1:c.475+105A>G XP_011525848.1:n.475+105A>G
XM_011527547.1:c.350A>G XP_011525849.1:p.Gln117Arg
XM_005259441.4:c.212A>G XP_005259498.2:p.Gln71Arg
XM_011527545.3:c.493A>G XP_011525847.1:p.Ser165Gly
XM_011527546.2:c.475+105A>G XP_011525848.1:n.475+105A>G
NM_001302961.2:c.212A>G NP_001289890.1:p.Gln71Arg
NR_126566.2:n.486A>G
NM_004917.5:c.497A>G MANE Select NP_004908.4:p.Gln166Arg