Canonical Allele Identifier: CA508211771

Gene: KLK4

Linked Data

• MyVariant Identifiers: chr19:g.51411621G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908365G>A , CM000681.2:g.50908365G>A	GRCh38
NC_000019.9:g.51411621G>A , CM000681.1:g.51411621G>A	GRCh37
NC_000019.8:g.56103433G>A	NCBI36
NG_012154.2:g.7374C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.606C>T MANE Select	ENSP00000326159.1:p.Ser202=
ENST00000324041.5:c.606C>T	ENSP00000326159.1:p.Ser202=
ENST00000431178.2:c.328+214C>T	ENSP00000399448.2:n.328+214C>T
ENST00000593885.1:c.*101C>T	ENSP00000469769.1:n.*101C>T
ENST00000596876.1:n.608C>T
ENST00000598305.5:c.*101C>T	ENSP00000469963.1:n.*101C>T
ENST00000599865.5:n.542C>T
ENST00000602148.1:c.618C>T	ENSP00000472091.1:n.618C>T
NM_001302961.1:c.321C>T	NP_001289890.1:p.Ser107=
NM_004917.4:c.606C>T	NP_004908.4:p.Ser202=
NR_126566.1:n.595C>T
XM_005259441.3:c.321C>T	XP_005259498.2:p.Ser107=
XM_011527546.1:c.475+214C>T	XP_011525848.1:n.475+214C>T
XM_011527547.1:c.459C>T	XP_011525849.1:p.Ser153=
XM_005259441.4:c.321C>T	XP_005259498.2:p.Ser107=
XM_011527546.2:c.475+214C>T	XP_011525848.1:n.475+214C>T
NM_001302961.2:c.321C>T	NP_001289890.1:p.Ser107=
NR_126566.2:n.595C>T
NM_004917.5:c.606C>T MANE Select	NP_004908.4:p.Ser202=