Canonical Allele Identifier: CA407041387

Gene: KLK4

Linked Data

• MyVariant Identifiers: chr19:g.51411876C>G (hg19) ; chr19:g.50908620C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908620C>G , CM000681.2:g.50908620C>G	GRCh38
NC_000019.9:g.51411876C>G , CM000681.1:g.51411876C>G	GRCh37
NC_000019.8:g.56103688C>G	NCBI36
NG_012154.2:g.7119G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.434G>C MANE Select	ENSP00000326159.1:p.Gly145Ala
ENST00000324041.5:c.434G>C	ENSP00000326159.1:p.Gly145Ala
ENST00000431178.2:c.287G>C	ENSP00000399448.2:p.Gly96Ala
ENST00000593885.1:c.149G>C	ENSP00000469769.1:p.Gly50Ala
ENST00000596876.1:n.353G>C
ENST00000598305.5:c.149G>C	ENSP00000469963.1:p.Gly50Ala
ENST00000599865.5:n.287G>C
ENST00000602148.1:c.446G>C	ENSP00000472091.1:n.446G>C
NM_001302961.1:c.149G>C	NP_001289890.1:p.Gly50Ala
NM_004917.4:c.434G>C	NP_004908.4:p.Gly145Ala
NR_126566.1:n.427G>C
XM_005259441.3:c.149G>C	XP_005259498.2:p.Gly50Ala
XM_011527545.1:c.434G>C	XP_011525847.1:p.Gly145Ala
XM_011527546.1:c.434G>C	XP_011525848.1:p.Gly145Ala
XM_011527547.1:c.287G>C	XP_011525849.1:p.Gly96Ala
XM_005259441.4:c.149G>C	XP_005259498.2:p.Gly50Ala
XM_011527545.3:c.434G>C	XP_011525847.1:p.Gly145Ala
XM_011527546.2:c.434G>C	XP_011525848.1:p.Gly145Ala
NM_001302961.2:c.149G>C	NP_001289890.1:p.Gly50Ala
NR_126566.2:n.427G>C
NM_004917.5:c.434G>C MANE Select	NP_004908.4:p.Gly145Ala