Canonical Allele Identifier: CA407041186

Gene: KLK4

Linked Data

• MyVariant Identifiers: chr19:g.51411746T>C (hg19) ; chr19:g.50908490T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908490T>C , CM000681.2:g.50908490T>C	GRCh38
NC_000019.9:g.51411746T>C , CM000681.1:g.51411746T>C	GRCh37
NC_000019.8:g.56103558T>C	NCBI36
NG_012154.2:g.7249A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.481A>G MANE Select	ENSP00000326159.1:p.Met161Val
ENST00000324041.5:c.481A>G	ENSP00000326159.1:p.Met161Val
ENST00000431178.2:c.328+89A>G	ENSP00000399448.2:n.328+89A>G
ENST00000593885.1:c.192A>G	ENSP00000469769.1:p.Glu64=
ENST00000596876.1:n.483A>G
ENST00000598305.5:c.192A>G	ENSP00000469963.1:p.Glu64=
ENST00000599865.5:n.417A>G
ENST00000602148.1:c.493A>G	ENSP00000472091.1:n.493A>G
NM_001302961.1:c.196A>G	NP_001289890.1:p.Met66Val
NM_004917.4:c.481A>G	NP_004908.4:p.Met161Val
NR_126566.1:n.470A>G
XM_005259441.3:c.196A>G	XP_005259498.2:p.Met66Val
XM_011527545.1:c.477A>G	XP_011525847.1:p.Glu159=
XM_011527546.1:c.475+89A>G	XP_011525848.1:n.475+89A>G
XM_011527547.1:c.334A>G	XP_011525849.1:p.Met112Val
XM_005259441.4:c.196A>G	XP_005259498.2:p.Met66Val
XM_011527545.3:c.477A>G	XP_011525847.1:p.Glu159=
XM_011527546.2:c.475+89A>G	XP_011525848.1:n.475+89A>G
NM_001302961.2:c.196A>G	NP_001289890.1:p.Met66Val
NR_126566.2:n.470A>G
NM_004917.5:c.481A>G MANE Select	NP_004908.4:p.Met161Val