Canonical Allele Identifier: CA507833911

Gene: SIX5

Linked Data

• MyVariant Identifiers: chr19:g.46270299C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45767041C>A , CM000681.2:g.45767041C>A	GRCh38
NC_000019.9:g.46270299C>A , CM000681.1:g.46270299C>A	GRCh37
NC_000019.8:g.50962139C>A	NCBI36
NG_012745.1:g.7199G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317578.7:c.918G>T MANE Select	ENSP00000316842.4:p.Leu306=
ENST00000317578.6:c.918G>T	ENSP00000316842.4:p.Leu306=
ENST00000560160.1:c.587-930G>T
ENST00000560168.1:c.*106G>T	ENSP00000453189.2:n.*106G>T
ENST00000622857.1:c.16-1079G>T	ENSP00000481365.1:n.16-1079G>T
NM_175875.4:c.918G>T	NP_787071.2:p.Leu306=
NM_175875.5:c.918G>T MANE Select	NP_787071.3:p.Leu306=