Canonical Allele Identifier: CA407040633

Gene: KLK4

Linked Data

• MyVariant Identifiers: chr19:g.51411683A>G (hg19) ; chr19:g.50908427A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908427A>G , CM000681.2:g.50908427A>G	GRCh38
NC_000019.9:g.51411683A>G , CM000681.1:g.51411683A>G	GRCh37
NC_000019.8:g.56103495A>G	NCBI36
NG_012154.2:g.7312T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.544T>C MANE Select	ENSP00000326159.1:p.Tyr182His
ENST00000324041.5:c.544T>C	ENSP00000326159.1:p.Tyr182His
ENST00000431178.2:c.328+152T>C	ENSP00000399448.2:n.328+152T>C
ENST00000593885.1:c.*39T>C	ENSP00000469769.1:n.*39T>C
ENST00000596876.1:n.546T>C
ENST00000598305.5:c.*39T>C	ENSP00000469963.1:n.*39T>C
ENST00000599865.5:n.480T>C
ENST00000602148.1:c.556T>C	ENSP00000472091.1:n.556T>C
NM_001302961.1:c.259T>C	NP_001289890.1:p.Tyr87His
NM_004917.4:c.544T>C	NP_004908.4:p.Tyr182His
NR_126566.1:n.533T>C
XM_005259441.3:c.259T>C	XP_005259498.2:p.Tyr87His
XM_011527545.1:c.*39T>C	XP_011525847.1:n.*39T>C
XM_011527546.1:c.475+152T>C	XP_011525848.1:n.475+152T>C
XM_011527547.1:c.397T>C	XP_011525849.1:p.Tyr133His
XM_005259441.4:c.259T>C	XP_005259498.2:p.Tyr87His
XM_011527545.3:c.*39T>C	XP_011525847.1:n.*39T>C
XM_011527546.2:c.475+152T>C	XP_011525848.1:n.475+152T>C
NM_001302961.2:c.259T>C	NP_001289890.1:p.Tyr87His
NR_126566.2:n.533T>C
NM_004917.5:c.544T>C MANE Select	NP_004908.4:p.Tyr182His