Canonical Allele Identifier: CA491170343

Gene: STRA6

Linked Data

• MyVariant Identifiers: chr15:g.74472529G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74180188G>C , CM000677.2:g.74180188G>C	GRCh38
NC_000015.9:g.74472529G>C , CM000677.1:g.74472529G>C	GRCh37
NC_000015.8:g.72259582G>C	NCBI36
NG_009207.1:g.33843C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395105.9:c.1896C>G MANE Select	ENSP00000378537.4:p.Ala632=
ENST00000323940.9:c.1896C>G	ENSP00000326085.5:p.Ala632=
ENST00000395105.8:c.1896C>G	ENSP00000378537.4:p.Ala632=
ENST00000416286.7:c.1872C>G	ENSP00000400403.3:p.Ala624=
ENST00000423167.6:c.1869C>G	ENSP00000413012.2:p.Ala623=
ENST00000449139.6:c.1896C>G	ENSP00000410221.2:p.Ala632=
ENST00000535552.5:c.2007C>G	ENSP00000440238.1:p.Ala669=
ENST00000545137.5:n.1605C>G
ENST00000563965.5:c.2013C>G	ENSP00000456609.1:p.Ala671=
ENST00000572785.1:c.751C>G
ENST00000574278.5:c.1941C>G	ENSP00000458827.1:p.Ala647=
ENST00000574439.5:n.2168C>G
ENST00000616000.4:c.1896C>G	ENSP00000479112.1:p.Ala632=
NM_001142617.1:c.1896C>G	NP_001136089.1:p.Ala632=
NM_001142618.1:c.1896C>G	NP_001136090.1:p.Ala632=
NM_001142619.1:c.1869C>G	NP_001136091.1:p.Ala623=
NM_001199040.1:c.2007C>G	NP_001185969.1:p.Ala669=
NM_001199041.1:c.1941C>G	NP_001185970.1:p.Ala647=
NM_001199042.1:c.2013C>G	NP_001185971.1:p.Ala671=
NM_022369.3:c.1896C>G	NP_071764.3:p.Ala632=
XM_011521883.1:c.1896C>G	XP_011520185.1:p.Ala632=
XM_011521884.1:c.1707C>G	XP_011520186.1:p.Ala569=
XM_017022478.1:c.1944C>G	XP_016877967.1:p.Ala648=
XM_017022479.1:c.1896C>G	XP_016877968.1:p.Ala632=
XM_017022480.1:c.1707C>G	XP_016877969.1:p.Ala569=
NM_022369.4:c.1896C>G MANE Select	NP_071764.3:p.Ala632=
NM_001142617.2:c.1896C>G	NP_001136089.1:p.Ala632=
NM_001142619.2:c.1869C>G	NP_001136091.1:p.Ala623=
NM_001199042.2:c.2013C>G	NP_001185971.1:p.Ala671=
NM_001142618.2:c.1896C>G	NP_001136090.1:p.Ala632=
NM_001199040.2:c.2007C>G	NP_001185969.1:p.Ala669=
NM_001199041.2:c.1941C>G	NP_001185970.1:p.Ala647=