Canonical Allele Identifier: CA508313910
Gene: KLK4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.51412069G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50908813G>A , CM000681.2:g.50908813G>A GRCh38
NC_000019.9:g.51412069G>A , CM000681.1:g.51412069G>A GRCh37
NC_000019.8:g.56103881G>A NCBI36
NG_012154.2:g.6926C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000324041.6:c.241C>T MANE Select ENSP00000326159.1:p.Leu81=
ENST00000324041.5:c.241C>T ENSP00000326159.1:p.Leu81=
ENST00000431178.2:c.94C>T ENSP00000399448.2:p.Leu32=
ENST00000593885.1:c.-45C>T ENSP00000469769.1:n.-45C>T
ENST00000596876.1:n.160C>T
ENST00000598305.5:c.-45C>T ENSP00000469963.1:n.-45C>T
ENST00000599865.5:n.94C>T
ENST00000602148.1:c.253C>T ENSP00000472091.1:n.253C>T
NM_001302961.1:c.-45C>T NP_001289890.1:n.-45C>T
NM_004917.4:c.241C>T NP_004908.4:p.Leu81=
NR_126566.1:n.234C>T
XM_005259441.3:c.-45C>T XP_005259498.2:n.-45C>T
XM_011527545.1:c.241C>T XP_011525847.1:p.Leu81=
XM_011527546.1:c.241C>T XP_011525848.1:p.Leu81=
XM_011527547.1:c.94C>T XP_011525849.1:p.Leu32=
XM_005259441.4:c.-45C>T XP_005259498.2:n.-45C>T
XM_011527545.3:c.241C>T XP_011525847.1:p.Leu81=
XM_011527546.2:c.241C>T XP_011525848.1:p.Leu81=
NM_001302961.2:c.-45C>T NP_001289890.1:n.-45C>T
NR_126566.2:n.234C>T
NM_004917.5:c.241C>T MANE Select NP_004908.4:p.Leu81=