Canonical Allele Identifier: CA407040644

Gene: KLK4

Linked Data

• MyVariant Identifiers: chr19:g.51411686G>A (hg19) ; chr19:g.50908430G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908430G>A , CM000681.2:g.50908430G>A	GRCh38
NC_000019.9:g.51411686G>A , CM000681.1:g.51411686G>A	GRCh37
NC_000019.8:g.56103498G>A	NCBI36
NG_012154.2:g.7309C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.541C>T MANE Select	ENSP00000326159.1:p.Leu181Phe
ENST00000324041.5:c.541C>T	ENSP00000326159.1:p.Leu181Phe
ENST00000431178.2:c.328+149C>T	ENSP00000399448.2:n.328+149C>T
ENST00000593885.1:c.*36C>T	ENSP00000469769.1:n.*36C>T
ENST00000596876.1:n.543C>T
ENST00000598305.5:c.*36C>T	ENSP00000469963.1:n.*36C>T
ENST00000599865.5:n.477C>T
ENST00000602148.1:c.553C>T	ENSP00000472091.1:n.553C>T
NM_001302961.1:c.256C>T	NP_001289890.1:p.Leu86Phe
NM_004917.4:c.541C>T	NP_004908.4:p.Leu181Phe
NR_126566.1:n.530C>T
XM_005259441.3:c.256C>T	XP_005259498.2:p.Leu86Phe
XM_011527545.1:c.*36C>T	XP_011525847.1:n.*36C>T
XM_011527546.1:c.475+149C>T	XP_011525848.1:n.475+149C>T
XM_011527547.1:c.394C>T	XP_011525849.1:p.Leu132Phe
XM_005259441.4:c.256C>T	XP_005259498.2:p.Leu86Phe
XM_011527545.3:c.*36C>T	XP_011525847.1:n.*36C>T
XM_011527546.2:c.475+149C>T	XP_011525848.1:n.475+149C>T
NM_001302961.2:c.256C>T	NP_001289890.1:p.Leu86Phe
NR_126566.2:n.530C>T
NM_004917.5:c.541C>T MANE Select	NP_004908.4:p.Leu181Phe