Canonical Allele Identifier: CA508313831
Gene: KLK4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.51412004G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50908748G>T , CM000681.2:g.50908748G>T GRCh38
NC_000019.9:g.51412004G>T , CM000681.1:g.51412004G>T GRCh37
NC_000019.8:g.56103816G>T NCBI36
NG_012154.2:g.6991C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000324041.6:c.306C>A MANE Select ENSP00000326159.1:p.Ser102=
ENST00000324041.5:c.306C>A ENSP00000326159.1:p.Ser102=
ENST00000431178.2:c.159C>A ENSP00000399448.2:p.Ser53=
ENST00000593885.1:c.21C>A ENSP00000469769.1:p.Ser7=
ENST00000596876.1:n.225C>A
ENST00000598305.5:c.21C>A ENSP00000469963.1:p.Ser7=
ENST00000599865.5:n.159C>A
ENST00000602148.1:c.318C>A ENSP00000472091.1:n.318C>A
NM_001302961.1:c.21C>A NP_001289890.1:p.Ser7=
NM_004917.4:c.306C>A NP_004908.4:p.Ser102=
NR_126566.1:n.299C>A
XM_005259441.3:c.21C>A XP_005259498.2:p.Ser7=
XM_011527545.1:c.306C>A XP_011525847.1:p.Ser102=
XM_011527546.1:c.306C>A XP_011525848.1:p.Ser102=
XM_011527547.1:c.159C>A XP_011525849.1:p.Ser53=
XM_005259441.4:c.21C>A XP_005259498.2:p.Ser7=
XM_011527545.3:c.306C>A XP_011525847.1:p.Ser102=
XM_011527546.2:c.306C>A XP_011525848.1:p.Ser102=
NM_001302961.2:c.21C>A NP_001289890.1:p.Ser7=
NR_126566.2:n.299C>A
NM_004917.5:c.306C>A MANE Select NP_004908.4:p.Ser102=