Canonical Allele Identifier: CA9605048

Gene: KLK4

Linked Data

• dbSNP Id: rs763799687
• ExAC: 19:51411768 T / G
• gnomAD v2: 19-51411768-T-G
• gnomAD v4: 19-50908512-T-G
• MyVariant Identifiers: chr19:g.51411768T>G (hg19) ; chr19:g.50908512T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908512T>G , CM000681.2:g.50908512T>G	GRCh38
NC_000019.9:g.51411768T>G , CM000681.1:g.51411768T>G	GRCh37
NC_000019.8:g.56103580T>G	NCBI36
NG_012154.2:g.7227A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000324041.6:c.476-17A>C MANE Select	ENSP00000326159.1:n.476-17A>C
ENST00000324041.5:c.476-17A>C	ENSP00000326159.1:n.476-17A>C
ENST00000431178.2:c.328+67A>C	ENSP00000399448.2:n.328+67A>C
ENST00000593885.1:c.191-21A>C	ENSP00000469769.1:n.191-21A>C
ENST00000596876.1:n.461A>C
ENST00000598305.5:c.191-21A>C	ENSP00000469963.1:n.191-21A>C
ENST00000599865.5:n.395A>C
ENST00000602148.1:c.488-17A>C	ENSP00000472091.1:n.488-17A>C
NM_001302961.1:c.191-17A>C	NP_001289890.1:n.191-17A>C
NM_004917.4:c.476-17A>C	NP_004908.4:n.476-17A>C
NR_126566.1:n.469-21A>C
XM_005259441.3:c.191-17A>C	XP_005259498.2:n.191-17A>C
XM_011527545.1:c.476-21A>C	XP_011525847.1:n.476-21A>C
XM_011527546.1:c.475+67A>C	XP_011525848.1:n.475+67A>C
XM_011527547.1:c.329-17A>C	XP_011525849.1:n.329-17A>C
XM_005259441.4:c.191-17A>C	XP_005259498.2:n.191-17A>C
XM_011527545.3:c.476-21A>C	XP_011525847.1:n.476-21A>C
XM_011527546.2:c.475+67A>C	XP_011525848.1:n.475+67A>C
NM_001302961.2:c.191-17A>C	NP_001289890.1:n.191-17A>C
NR_126566.2:n.469-21A>C
NM_004917.5:c.476-17A>C MANE Select	NP_004908.4:n.476-17A>C