Canonical Allele Identifier: CA407041852

Gene: KLK4

Linked Data

• MyVariant Identifiers: chr19:g.51412075T>A (hg19) ; chr19:g.50908819T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908819T>A , CM000681.2:g.50908819T>A	GRCh38
NC_000019.9:g.51412075T>A , CM000681.1:g.51412075T>A	GRCh37
NC_000019.8:g.56103887T>A	NCBI36
NG_012154.2:g.6920A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.235A>T MANE Select	ENSP00000326159.1:p.Ile79Phe
ENST00000324041.5:c.235A>T	ENSP00000326159.1:p.Ile79Phe
ENST00000431178.2:c.88A>T	ENSP00000399448.2:p.Ile30Phe
ENST00000593885.1:c.-51A>T	ENSP00000469769.1:n.-51A>T
ENST00000596876.1:n.154A>T
ENST00000598305.5:c.-51A>T	ENSP00000469963.1:n.-51A>T
ENST00000599865.5:n.88A>T
ENST00000602148.1:c.247A>T	ENSP00000472091.1:n.247A>T
NM_001302961.1:c.-51A>T	NP_001289890.1:n.-51A>T
NM_004917.4:c.235A>T	NP_004908.4:p.Ile79Phe
NR_126566.1:n.228A>T
XM_005259441.3:c.-51A>T	XP_005259498.2:n.-51A>T
XM_011527545.1:c.235A>T	XP_011525847.1:p.Ile79Phe
XM_011527546.1:c.235A>T	XP_011525848.1:p.Ile79Phe
XM_011527547.1:c.88A>T	XP_011525849.1:p.Ile30Phe
XM_005259441.4:c.-51A>T	XP_005259498.2:n.-51A>T
XM_011527545.3:c.235A>T	XP_011525847.1:p.Ile79Phe
XM_011527546.2:c.235A>T	XP_011525848.1:p.Ile79Phe
NM_001302961.2:c.-51A>T	NP_001289890.1:n.-51A>T
NR_126566.2:n.228A>T
NM_004917.5:c.235A>T MANE Select	NP_004908.4:p.Ile79Phe