Canonical Allele Identifier: CA407040823

Gene: KLK4

Linked Data

• MyVariant Identifiers: chr19:g.51411716A>C (hg19) ; chr19:g.50908460A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908460A>C , CM000681.2:g.50908460A>C	GRCh38
NC_000019.9:g.51411716A>C , CM000681.1:g.51411716A>C	GRCh37
NC_000019.8:g.56103528A>C	NCBI36
NG_012154.2:g.7279T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.511T>G MANE Select	ENSP00000326159.1:p.Ser171Ala
ENST00000324041.5:c.511T>G	ENSP00000326159.1:p.Ser171Ala
ENST00000431178.2:c.328+119T>G	ENSP00000399448.2:n.328+119T>G
ENST00000593885.1:c.*6T>G	ENSP00000469769.1:n.*6T>G
ENST00000596876.1:n.513T>G
ENST00000598305.5:c.*6T>G	ENSP00000469963.1:n.*6T>G
ENST00000599865.5:n.447T>G
ENST00000602148.1:c.523T>G	ENSP00000472091.1:n.523T>G
NM_001302961.1:c.226T>G	NP_001289890.1:p.Ser76Ala
NM_004917.4:c.511T>G	NP_004908.4:p.Ser171Ala
NR_126566.1:n.500T>G
XM_005259441.3:c.226T>G	XP_005259498.2:p.Ser76Ala
XM_011527545.1:c.*6T>G	XP_011525847.1:n.*6T>G
XM_011527546.1:c.475+119T>G	XP_011525848.1:n.475+119T>G
XM_011527547.1:c.364T>G	XP_011525849.1:p.Ser122Ala
XM_005259441.4:c.226T>G	XP_005259498.2:p.Ser76Ala
XM_011527545.3:c.*6T>G	XP_011525847.1:n.*6T>G
XM_011527546.2:c.475+119T>G	XP_011525848.1:n.475+119T>G
NM_001302961.2:c.226T>G	NP_001289890.1:p.Ser76Ala
NR_126566.2:n.500T>G
NM_004917.5:c.511T>G MANE Select	NP_004908.4:p.Ser171Ala