Canonical Allele Identifier: CA407040341
Gene: KLK4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50908378T>C , CM000681.2:g.50908378T>C GRCh38
NC_000019.9:g.51411634T>C , CM000681.1:g.51411634T>C GRCh37
NC_000019.8:g.56103446T>C NCBI36
NG_012154.2:g.7361A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000324041.6:c.593A>G MANE Select ENSP00000326159.1:p.Asp198Gly
ENST00000324041.5:c.593A>G ENSP00000326159.1:p.Asp198Gly
ENST00000431178.2:c.328+201A>G ENSP00000399448.2:n.328+201A>G
ENST00000593885.1:c.*88A>G ENSP00000469769.1:n.*88A>G
ENST00000596876.1:n.595A>G
ENST00000598305.5:c.*88A>G ENSP00000469963.1:n.*88A>G
ENST00000599865.5:n.529A>G
ENST00000602148.1:c.605A>G ENSP00000472091.1:n.605A>G
NM_001302961.1:c.308A>G NP_001289890.1:p.Asp103Gly
NM_004917.4:c.593A>G NP_004908.4:p.Asp198Gly
NR_126566.1:n.582A>G
XM_005259441.3:c.308A>G XP_005259498.2:p.Asp103Gly
XM_011527546.1:c.475+201A>G XP_011525848.1:n.475+201A>G
XM_011527547.1:c.446A>G XP_011525849.1:p.Asp149Gly
XM_005259441.4:c.308A>G XP_005259498.2:p.Asp103Gly
XM_011527545.3:c.*88A>G XP_011525847.1:n.*88A>G
XM_011527546.2:c.475+201A>G XP_011525848.1:n.475+201A>G
NM_001302961.2:c.308A>G NP_001289890.1:p.Asp103Gly
NR_126566.2:n.582A>G
NM_004917.5:c.593A>G MANE Select NP_004908.4:p.Asp198Gly