Canonical Allele Identifier: CA508313847

Gene: KLK4

Linked Data

• MyVariant Identifiers: chr19:g.51412013G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908757G>C , CM000681.2:g.50908757G>C	GRCh38
NC_000019.9:g.51412013G>C , CM000681.1:g.51412013G>C	GRCh37
NC_000019.8:g.56103825G>C	NCBI36
NG_012154.2:g.6982C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.297C>G MANE Select	ENSP00000326159.1:p.Ala99=
ENST00000324041.5:c.297C>G	ENSP00000326159.1:p.Ala99=
ENST00000431178.2:c.150C>G	ENSP00000399448.2:p.Ala50=
ENST00000593885.1:c.12C>G	ENSP00000469769.1:p.Ala4=
ENST00000596876.1:n.216C>G
ENST00000598305.5:c.12C>G	ENSP00000469963.1:p.Ala4=
ENST00000599865.5:n.150C>G
ENST00000602148.1:c.309C>G	ENSP00000472091.1:n.309C>G
NM_001302961.1:c.12C>G	NP_001289890.1:p.Ala4=
NM_004917.4:c.297C>G	NP_004908.4:p.Ala99=
NR_126566.1:n.290C>G
XM_005259441.3:c.12C>G	XP_005259498.2:p.Ala4=
XM_011527545.1:c.297C>G	XP_011525847.1:p.Ala99=
XM_011527546.1:c.297C>G	XP_011525848.1:p.Ala99=
XM_011527547.1:c.150C>G	XP_011525849.1:p.Ala50=
XM_005259441.4:c.12C>G	XP_005259498.2:p.Ala4=
XM_011527545.3:c.297C>G	XP_011525847.1:p.Ala99=
XM_011527546.2:c.297C>G	XP_011525848.1:p.Ala99=
NM_001302961.2:c.12C>G	NP_001289890.1:p.Ala4=
NR_126566.2:n.290C>G
NM_004917.5:c.297C>G MANE Select	NP_004908.4:p.Ala99=