Canonical Allele Identifier: CA491170283

Gene: STRA6

Linked Data

• MyVariant Identifiers: chr15:g.74472451G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74180110G>T , CM000677.2:g.74180110G>T	GRCh38
NC_000015.9:g.74472451G>T , CM000677.1:g.74472451G>T	GRCh37
NC_000015.8:g.72259504G>T	NCBI36
NG_009207.1:g.33921C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395105.9:c.1974C>A MANE Select	ENSP00000378537.4:p.Ala658=
ENST00000323940.9:c.1974C>A	ENSP00000326085.5:p.Ala658=
ENST00000395105.8:c.1974C>A	ENSP00000378537.4:p.Ala658=
ENST00000416286.7:c.1950C>A	ENSP00000400403.3:p.Ala650=
ENST00000423167.6:c.1947C>A	ENSP00000413012.2:p.Ala649=
ENST00000449139.6:c.1974C>A	ENSP00000410221.2:p.Ala658=
ENST00000535552.5:c.2085C>A	ENSP00000440238.1:p.Ala695=
ENST00000545137.5:n.1683C>A
ENST00000563965.5:c.2091C>A	ENSP00000456609.1:p.Ala697=
ENST00000574278.5:c.2019C>A	ENSP00000458827.1:p.Ala673=
ENST00000574439.5:n.2246C>A
ENST00000616000.4:c.1974C>A	ENSP00000479112.1:p.Ala658=
NM_001142617.1:c.1974C>A	NP_001136089.1:p.Ala658=
NM_001142618.1:c.1974C>A	NP_001136090.1:p.Ala658=
NM_001142619.1:c.1947C>A	NP_001136091.1:p.Ala649=
NM_001199040.1:c.2085C>A	NP_001185969.1:p.Ala695=
NM_001199041.1:c.2019C>A	NP_001185970.1:p.Ala673=
NM_001199042.1:c.2091C>A	NP_001185971.1:p.Ala697=
NM_022369.3:c.1974C>A	NP_071764.3:p.Ala658=
XM_011521883.1:c.1974C>A	XP_011520185.1:p.Ala658=
XM_011521884.1:c.1785C>A	XP_011520186.1:p.Ala595=
XM_017022478.1:c.2022C>A	XP_016877967.1:p.Ala674=
XM_017022479.1:c.1974C>A	XP_016877968.1:p.Ala658=
XM_017022480.1:c.1785C>A	XP_016877969.1:p.Ala595=
NM_022369.4:c.1974C>A MANE Select	NP_071764.3:p.Ala658=
NM_001142617.2:c.1974C>A	NP_001136089.1:p.Ala658=
NM_001142619.2:c.1947C>A	NP_001136091.1:p.Ala649=
NM_001199042.2:c.2091C>A	NP_001185971.1:p.Ala697=
NM_001142618.2:c.1974C>A	NP_001136090.1:p.Ala658=
NM_001199040.2:c.2085C>A	NP_001185969.1:p.Ala695=
NM_001199041.2:c.2019C>A	NP_001185970.1:p.Ala673=