Canonical Allele Identifier: CA407040415

Gene: KLK4

Linked Data

• MyVariant Identifiers: chr19:g.51411649G>C (hg19) ; chr19:g.50908393G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908393G>C , CM000681.2:g.50908393G>C	GRCh38
NC_000019.9:g.51411649G>C , CM000681.1:g.51411649G>C	GRCh37
NC_000019.8:g.56103461G>C	NCBI36
NG_012154.2:g.7346C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.578C>G MANE Select	ENSP00000326159.1:p.Ala193Gly
ENST00000324041.5:c.578C>G	ENSP00000326159.1:p.Ala193Gly
ENST00000431178.2:c.328+186C>G	ENSP00000399448.2:n.328+186C>G
ENST00000593885.1:c.*73C>G	ENSP00000469769.1:n.*73C>G
ENST00000596876.1:n.580C>G
ENST00000598305.5:c.*73C>G	ENSP00000469963.1:n.*73C>G
ENST00000599865.5:n.514C>G
ENST00000602148.1:c.590C>G	ENSP00000472091.1:n.590C>G
NM_001302961.1:c.293C>G	NP_001289890.1:p.Ala98Gly
NM_004917.4:c.578C>G	NP_004908.4:p.Ala193Gly
NR_126566.1:n.567C>G
XM_005259441.3:c.293C>G	XP_005259498.2:p.Ala98Gly
XM_011527545.1:c.*73C>G	XP_011525847.1:n.*73C>G
XM_011527546.1:c.475+186C>G	XP_011525848.1:n.475+186C>G
XM_011527547.1:c.431C>G	XP_011525849.1:p.Ala144Gly
XM_005259441.4:c.293C>G	XP_005259498.2:p.Ala98Gly
XM_011527545.3:c.*73C>G	XP_011525847.1:n.*73C>G
XM_011527546.2:c.475+186C>G	XP_011525848.1:n.475+186C>G
NM_001302961.2:c.293C>G	NP_001289890.1:p.Ala98Gly
NR_126566.2:n.567C>G
NM_004917.5:c.578C>G MANE Select	NP_004908.4:p.Ala193Gly