Canonical Allele Identifier: CA491170416

Gene: STRA6

Linked Data

• gnomAD v4: 15-74180783-T-C
• MyVariant Identifiers: chr15:g.74473124T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74180783T>C , CM000677.2:g.74180783T>C	GRCh38
NC_000015.9:g.74473124T>C , CM000677.1:g.74473124T>C	GRCh37
NC_000015.8:g.72260177T>C	NCBI36
NG_009207.1:g.33248A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395105.9:c.1839A>G MANE Select	ENSP00000378537.4:p.Glu613=
ENST00000323940.9:c.1839A>G	ENSP00000326085.5:p.Glu613=
ENST00000395105.8:c.1839A>G	ENSP00000378537.4:p.Glu613=
ENST00000416286.7:c.1815A>G	ENSP00000400403.3:p.Glu605=
ENST00000423167.6:c.1812A>G	ENSP00000413012.2:p.Glu604=
ENST00000449139.6:c.1839A>G	ENSP00000410221.2:p.Glu613=
ENST00000535552.5:c.1950A>G	ENSP00000440238.1:p.Glu650=
ENST00000545137.5:n.1548A>G
ENST00000563965.5:c.1956A>G	ENSP00000456609.1:p.Glu652=
ENST00000572785.1:c.694A>G
ENST00000574278.5:c.1884A>G	ENSP00000458827.1:p.Glu628=
ENST00000574439.5:n.2111A>G
ENST00000616000.4:c.1839A>G	ENSP00000479112.1:p.Glu613=
NM_001142617.1:c.1839A>G	NP_001136089.1:p.Glu613=
NM_001142618.1:c.1839A>G	NP_001136090.1:p.Glu613=
NM_001142619.1:c.1812A>G	NP_001136091.1:p.Glu604=
NM_001199040.1:c.1950A>G	NP_001185969.1:p.Glu650=
NM_001199041.1:c.1884A>G	NP_001185970.1:p.Glu628=
NM_001199042.1:c.1956A>G	NP_001185971.1:p.Glu652=
NM_022369.3:c.1839A>G	NP_071764.3:p.Glu613=
XM_011521883.1:c.1839A>G	XP_011520185.1:p.Glu613=
XM_011521884.1:c.1650A>G	XP_011520186.1:p.Glu550=
XM_017022478.1:c.1887A>G	XP_016877967.1:p.Glu629=
XM_017022479.1:c.1839A>G	XP_016877968.1:p.Glu613=
XM_017022480.1:c.1650A>G	XP_016877969.1:p.Glu550=
NM_022369.4:c.1839A>G MANE Select	NP_071764.3:p.Glu613=
NM_001142617.2:c.1839A>G	NP_001136089.1:p.Glu613=
NM_001142619.2:c.1812A>G	NP_001136091.1:p.Glu604=
NM_001199042.2:c.1956A>G	NP_001185971.1:p.Glu652=
NM_001142618.2:c.1839A>G	NP_001136090.1:p.Glu613=
NM_001199040.2:c.1950A>G	NP_001185969.1:p.Glu650=
NM_001199041.2:c.1884A>G	NP_001185970.1:p.Glu628=