Canonical Allele Identifier: CA406417492

Gene: SIX5

Linked Data

• MyVariant Identifiers: chr19:g.46269674T>A (hg19) ; chr19:g.45766416T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45766416T>A , CM000681.2:g.45766416T>A	GRCh38
NC_000019.9:g.46269674T>A , CM000681.1:g.46269674T>A	GRCh37
NC_000019.8:g.50961514T>A	NCBI36
NG_012745.1:g.7824A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317578.7:c.1543A>T MANE Select	ENSP00000316842.4:p.Asn515Tyr
ENST00000317578.6:c.1543A>T	ENSP00000316842.4:p.Asn515Tyr
ENST00000560160.1:c.587-305A>T
ENST00000560168.1:c.*731A>T	ENSP00000453189.2:n.*731A>T
ENST00000622857.1:c.16-454A>T	ENSP00000481365.1:n.16-454A>T
NM_175875.4:c.1543A>T	NP_787071.2:p.Asn515Tyr
NM_175875.5:c.1543A>T MANE Select	NP_787071.3:p.Asn515Tyr