Canonical Allele Identifier: CA407041321
Gene: KLK4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50908603A>T , CM000681.2:g.50908603A>T GRCh38
NC_000019.9:g.51411859A>T , CM000681.1:g.51411859A>T GRCh37
NC_000019.8:g.56103671A>T NCBI36
NG_012154.2:g.7136T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000324041.6:c.451T>A MANE Select ENSP00000326159.1:p.Ser151Thr
ENST00000324041.5:c.451T>A ENSP00000326159.1:p.Ser151Thr
ENST00000431178.2:c.304T>A ENSP00000399448.2:p.Ser102Thr
ENST00000593885.1:c.166T>A ENSP00000469769.1:p.Ser56Thr
ENST00000596876.1:n.370T>A
ENST00000598305.5:c.166T>A ENSP00000469963.1:p.Ser56Thr
ENST00000599865.5:n.304T>A
ENST00000602148.1:c.463T>A ENSP00000472091.1:n.463T>A
NM_001302961.1:c.166T>A NP_001289890.1:p.Ser56Thr
NM_004917.4:c.451T>A NP_004908.4:p.Ser151Thr
NR_126566.1:n.444T>A
XM_005259441.3:c.166T>A XP_005259498.2:p.Ser56Thr
XM_011527545.1:c.451T>A XP_011525847.1:p.Ser151Thr
XM_011527546.1:c.451T>A XP_011525848.1:p.Ser151Thr
XM_011527547.1:c.304T>A XP_011525849.1:p.Ser102Thr
XM_005259441.4:c.166T>A XP_005259498.2:p.Ser56Thr
XM_011527545.3:c.451T>A XP_011525847.1:p.Ser151Thr
XM_011527546.2:c.451T>A XP_011525848.1:p.Ser151Thr
NM_001302961.2:c.166T>A NP_001289890.1:p.Ser56Thr
NR_126566.2:n.444T>A
NM_004917.5:c.451T>A MANE Select NP_004908.4:p.Ser151Thr