Canonical Allele Identifier: CA407041396

Gene: KLK4

Linked Data

• MyVariant Identifiers: chr19:g.51411879G>C (hg19) ; chr19:g.50908623G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908623G>C , CM000681.2:g.50908623G>C	GRCh38
NC_000019.9:g.51411879G>C , CM000681.1:g.51411879G>C	GRCh37
NC_000019.8:g.56103691G>C	NCBI36
NG_012154.2:g.7116C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.431C>G MANE Select	ENSP00000326159.1:p.Ala144Gly
ENST00000324041.5:c.431C>G	ENSP00000326159.1:p.Ala144Gly
ENST00000431178.2:c.284C>G	ENSP00000399448.2:p.Ala95Gly
ENST00000593885.1:c.146C>G	ENSP00000469769.1:p.Ala49Gly
ENST00000596876.1:n.350C>G
ENST00000598305.5:c.146C>G	ENSP00000469963.1:p.Ala49Gly
ENST00000599865.5:n.284C>G
ENST00000602148.1:c.443C>G	ENSP00000472091.1:n.443C>G
NM_001302961.1:c.146C>G	NP_001289890.1:p.Ala49Gly
NM_004917.4:c.431C>G	NP_004908.4:p.Ala144Gly
NR_126566.1:n.424C>G
XM_005259441.3:c.146C>G	XP_005259498.2:p.Ala49Gly
XM_011527545.1:c.431C>G	XP_011525847.1:p.Ala144Gly
XM_011527546.1:c.431C>G	XP_011525848.1:p.Ala144Gly
XM_011527547.1:c.284C>G	XP_011525849.1:p.Ala95Gly
XM_005259441.4:c.146C>G	XP_005259498.2:p.Ala49Gly
XM_011527545.3:c.431C>G	XP_011525847.1:p.Ala144Gly
XM_011527546.2:c.431C>G	XP_011525848.1:p.Ala144Gly
NM_001302961.2:c.146C>G	NP_001289890.1:p.Ala49Gly
NR_126566.2:n.424C>G
NM_004917.5:c.431C>G MANE Select	NP_004908.4:p.Ala144Gly