Canonical Allele Identifier: CA407041800

Gene: KLK4

Linked Data

• MyVariant Identifiers: chr19:g.51412047G>T (hg19) ; chr19:g.50908791G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908791G>T , CM000681.2:g.50908791G>T	GRCh38
NC_000019.9:g.51412047G>T , CM000681.1:g.51412047G>T	GRCh37
NC_000019.8:g.56103859G>T	NCBI36
NG_012154.2:g.6948C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.263C>A MANE Select	ENSP00000326159.1:p.Ala88Asp
ENST00000324041.5:c.263C>A	ENSP00000326159.1:p.Ala88Asp
ENST00000431178.2:c.116C>A	ENSP00000399448.2:p.Ala39Asp
ENST00000593885.1:c.-23C>A	ENSP00000469769.1:n.-23C>A
ENST00000596876.1:n.182C>A
ENST00000598305.5:c.-23C>A	ENSP00000469963.1:n.-23C>A
ENST00000599865.5:n.116C>A
ENST00000602148.1:c.275C>A	ENSP00000472091.1:n.275C>A
NM_001302961.1:c.-23C>A	NP_001289890.1:n.-23C>A
NM_004917.4:c.263C>A	NP_004908.4:p.Ala88Asp
NR_126566.1:n.256C>A
XM_005259441.3:c.-23C>A	XP_005259498.2:n.-23C>A
XM_011527545.1:c.263C>A	XP_011525847.1:p.Ala88Asp
XM_011527546.1:c.263C>A	XP_011525848.1:p.Ala88Asp
XM_011527547.1:c.116C>A	XP_011525849.1:p.Ala39Asp
XM_005259441.4:c.-23C>A	XP_005259498.2:n.-23C>A
XM_011527545.3:c.263C>A	XP_011525847.1:p.Ala88Asp
XM_011527546.2:c.263C>A	XP_011525848.1:p.Ala88Asp
NM_001302961.2:c.-23C>A	NP_001289890.1:n.-23C>A
NR_126566.2:n.256C>A
NM_004917.5:c.263C>A MANE Select	NP_004908.4:p.Ala88Asp