Canonical Allele Identifier: CA508313844

Gene: KLK4

Linked Data

• MyVariant Identifiers: chr19:g.51411741A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908485A>G , CM000681.2:g.50908485A>G	GRCh38
NC_000019.9:g.51411741A>G , CM000681.1:g.51411741A>G	GRCh37
NC_000019.8:g.56103553A>G	NCBI36
NG_012154.2:g.7254T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.486T>C MANE Select	ENSP00000326159.1:p.Pro162=
ENST00000324041.5:c.486T>C	ENSP00000326159.1:p.Pro162=
ENST00000431178.2:c.328+94T>C	ENSP00000399448.2:n.328+94T>C
ENST00000593885.1:c.197T>C	ENSP00000469769.1:p.Leu66Pro
ENST00000596876.1:n.488T>C
ENST00000598305.5:c.197T>C	ENSP00000469963.1:p.Leu66Pro
ENST00000599865.5:n.422T>C
ENST00000602148.1:c.498T>C	ENSP00000472091.1:n.498T>C
NM_001302961.1:c.201T>C	NP_001289890.1:p.Pro67=
NM_004917.4:c.486T>C	NP_004908.4:p.Pro162=
NR_126566.1:n.475T>C
XM_005259441.3:c.201T>C	XP_005259498.2:p.Pro67=
XM_011527545.1:c.482T>C	XP_011525847.1:p.Leu161Pro
XM_011527546.1:c.475+94T>C	XP_011525848.1:n.475+94T>C
XM_011527547.1:c.339T>C	XP_011525849.1:p.Pro113=
XM_005259441.4:c.201T>C	XP_005259498.2:p.Pro67=
XM_011527545.3:c.482T>C	XP_011525847.1:p.Leu161Pro
XM_011527546.2:c.475+94T>C	XP_011525848.1:n.475+94T>C
NM_001302961.2:c.201T>C	NP_001289890.1:p.Pro67=
NR_126566.2:n.475T>C
NM_004917.5:c.486T>C MANE Select	NP_004908.4:p.Pro162=