Canonical Allele Identifier: CA393128163

Gene: STRA6

Linked Data

• MyVariant Identifiers: chr15:g.74472434C>A (hg19) ; chr15:g.74180093C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74180093C>A , CM000677.2:g.74180093C>A	GRCh38
NC_000015.9:g.74472434C>A , CM000677.1:g.74472434C>A	GRCh37
NC_000015.8:g.72259487C>A	NCBI36
NG_009207.1:g.33938G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395105.9:c.1991G>T MANE Select	ENSP00000378537.4:p.Gly664Val
ENST00000323940.9:c.1991G>T	ENSP00000326085.5:p.Gly664Val
ENST00000395105.8:c.1991G>T	ENSP00000378537.4:p.Gly664Val
ENST00000416286.7:c.1967G>T	ENSP00000400403.3:p.Gly656Val
ENST00000423167.6:c.1964G>T	ENSP00000413012.2:p.Gly655Val
ENST00000449139.6:c.1991G>T	ENSP00000410221.2:p.Gly664Val
ENST00000535552.5:c.2102G>T	ENSP00000440238.1:p.Gly701Val
ENST00000545137.5:n.1700G>T
ENST00000563965.5:c.2108G>T	ENSP00000456609.1:p.Gly703Val
ENST00000574278.5:c.2036G>T	ENSP00000458827.1:p.Gly679Val
ENST00000574439.5:n.2263G>T
ENST00000616000.4:c.1991G>T	ENSP00000479112.1:p.Gly664Val
NM_001142617.1:c.1991G>T	NP_001136089.1:p.Gly664Val
NM_001142618.1:c.1991G>T	NP_001136090.1:p.Gly664Val
NM_001142619.1:c.1964G>T	NP_001136091.1:p.Gly655Val
NM_001199040.1:c.2102G>T	NP_001185969.1:p.Gly701Val
NM_001199041.1:c.2036G>T	NP_001185970.1:p.Gly679Val
NM_001199042.1:c.2108G>T	NP_001185971.1:p.Gly703Val
NM_022369.3:c.1991G>T	NP_071764.3:p.Gly664Val
XM_011521883.1:c.1991G>T	XP_011520185.1:p.Gly664Val
XM_011521884.1:c.1802G>T	XP_011520186.1:p.Gly601Val
XM_017022478.1:c.2039G>T	XP_016877967.1:p.Gly680Val
XM_017022479.1:c.1991G>T	XP_016877968.1:p.Gly664Val
XM_017022480.1:c.1802G>T	XP_016877969.1:p.Gly601Val
NM_022369.4:c.1991G>T MANE Select	NP_071764.3:p.Gly664Val
NM_001142617.2:c.1991G>T	NP_001136089.1:p.Gly664Val
NM_001142619.2:c.1964G>T	NP_001136091.1:p.Gly655Val
NM_001199042.2:c.2108G>T	NP_001185971.1:p.Gly703Val
NM_001142618.2:c.1991G>T	NP_001136090.1:p.Gly664Val
NM_001199040.2:c.2102G>T	NP_001185969.1:p.Gly701Val
NM_001199041.2:c.2036G>T	NP_001185970.1:p.Gly679Val