Canonical Allele Identifier: CA407040360

Gene: KLK4

Linked Data

• MyVariant Identifiers: chr19:g.51411638G>A (hg19) ; chr19:g.50908382G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908382G>A , CM000681.2:g.50908382G>A	GRCh38
NC_000019.9:g.51411638G>A , CM000681.1:g.51411638G>A	GRCh37
NC_000019.8:g.56103450G>A	NCBI36
NG_012154.2:g.7357C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.589C>T MANE Select	ENSP00000326159.1:p.Gln197Ter
ENST00000324041.5:c.589C>T	ENSP00000326159.1:p.Gln197Ter
ENST00000431178.2:c.328+197C>T	ENSP00000399448.2:n.328+197C>T
ENST00000593885.1:c.*84C>T	ENSP00000469769.1:n.*84C>T
ENST00000596876.1:n.591C>T
ENST00000598305.5:c.*84C>T	ENSP00000469963.1:n.*84C>T
ENST00000599865.5:n.525C>T
ENST00000602148.1:c.601C>T	ENSP00000472091.1:n.601C>T
NM_001302961.1:c.304C>T	NP_001289890.1:p.Gln102Ter
NM_004917.4:c.589C>T	NP_004908.4:p.Gln197Ter
NR_126566.1:n.578C>T
XM_005259441.3:c.304C>T	XP_005259498.2:p.Gln102Ter
XM_011527546.1:c.475+197C>T	XP_011525848.1:n.475+197C>T
XM_011527547.1:c.442C>T	XP_011525849.1:p.Gln148Ter
XM_005259441.4:c.304C>T	XP_005259498.2:p.Gln102Ter
XM_011527545.3:c.*84C>T	XP_011525847.1:n.*84C>T
XM_011527546.2:c.475+197C>T	XP_011525848.1:n.475+197C>T
NM_001302961.2:c.304C>T	NP_001289890.1:p.Gln102Ter
NR_126566.2:n.578C>T
NM_004917.5:c.589C>T MANE Select	NP_004908.4:p.Gln197Ter