Canonical Allele Identifier: CA508313850

Gene: KLK4

Linked Data

• MyVariant Identifiers: chr19:g.51412019C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908763C>G , CM000681.2:g.50908763C>G	GRCh38
NC_000019.9:g.51412019C>G , CM000681.1:g.51412019C>G	GRCh37
NC_000019.8:g.56103831C>G	NCBI36
NG_012154.2:g.6976G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.291G>C MANE Select	ENSP00000326159.1:p.Val97=
ENST00000324041.5:c.291G>C	ENSP00000326159.1:p.Val97=
ENST00000431178.2:c.144G>C	ENSP00000399448.2:p.Val48=
ENST00000593885.1:c.6G>C	ENSP00000469769.1:p.Val2=
ENST00000596876.1:n.210G>C
ENST00000598305.5:c.6G>C	ENSP00000469963.1:p.Val2=
ENST00000599865.5:n.144G>C
ENST00000602148.1:c.303G>C	ENSP00000472091.1:n.303G>C
NM_001302961.1:c.6G>C	NP_001289890.1:p.Val2=
NM_004917.4:c.291G>C	NP_004908.4:p.Val97=
NR_126566.1:n.284G>C
XM_005259441.3:c.6G>C	XP_005259498.2:p.Val2=
XM_011527545.1:c.291G>C	XP_011525847.1:p.Val97=
XM_011527546.1:c.291G>C	XP_011525848.1:p.Val97=
XM_011527547.1:c.144G>C	XP_011525849.1:p.Val48=
XM_005259441.4:c.6G>C	XP_005259498.2:p.Val2=
XM_011527545.3:c.291G>C	XP_011525847.1:p.Val97=
XM_011527546.2:c.291G>C	XP_011525848.1:p.Val97=
NM_001302961.2:c.6G>C	NP_001289890.1:p.Val2=
NR_126566.2:n.284G>C
NM_004917.5:c.291G>C MANE Select	NP_004908.4:p.Val97=