Canonical Allele Identifier: CA407040467

Gene: KLK4

Linked Data

• MyVariant Identifiers: chr19:g.51411656A>G (hg19) ; chr19:g.50908400A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908400A>G , CM000681.2:g.50908400A>G	GRCh38
NC_000019.9:g.51411656A>G , CM000681.1:g.51411656A>G	GRCh37
NC_000019.8:g.56103468A>G	NCBI36
NG_012154.2:g.7339T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.571T>C MANE Select	ENSP00000326159.1:p.Phe191Leu
ENST00000324041.5:c.571T>C	ENSP00000326159.1:p.Phe191Leu
ENST00000431178.2:c.328+179T>C	ENSP00000399448.2:n.328+179T>C
ENST00000593885.1:c.*66T>C	ENSP00000469769.1:n.*66T>C
ENST00000596876.1:n.573T>C
ENST00000598305.5:c.*66T>C	ENSP00000469963.1:n.*66T>C
ENST00000599865.5:n.507T>C
ENST00000602148.1:c.583T>C	ENSP00000472091.1:n.583T>C
NM_001302961.1:c.286T>C	NP_001289890.1:p.Phe96Leu
NM_004917.4:c.571T>C	NP_004908.4:p.Phe191Leu
NR_126566.1:n.560T>C
XM_005259441.3:c.286T>C	XP_005259498.2:p.Phe96Leu
XM_011527545.1:c.*66T>C	XP_011525847.1:n.*66T>C
XM_011527546.1:c.475+179T>C	XP_011525848.1:n.475+179T>C
XM_011527547.1:c.424T>C	XP_011525849.1:p.Phe142Leu
XM_005259441.4:c.286T>C	XP_005259498.2:p.Phe96Leu
XM_011527545.3:c.*66T>C	XP_011525847.1:n.*66T>C
XM_011527546.2:c.475+179T>C	XP_011525848.1:n.475+179T>C
NM_001302961.2:c.286T>C	NP_001289890.1:p.Phe96Leu
NR_126566.2:n.560T>C
NM_004917.5:c.571T>C MANE Select	NP_004908.4:p.Phe191Leu