Canonical Allele Identifier: CA393128143

Gene: STRA6

Linked Data

• MyVariant Identifiers: chr15:g.74472423A>G (hg19) ; chr15:g.74180082A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74180082A>G , CM000677.2:g.74180082A>G	GRCh38
NC_000015.9:g.74472423A>G , CM000677.1:g.74472423A>G	GRCh37
NC_000015.8:g.72259476A>G	NCBI36
NG_009207.1:g.33949T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000395105.9:c.2002T>C MANE Select	ENSP00000378537.4:p.Ter668Arg
ENST00000323940.9:c.2002T>C	ENSP00000326085.5:p.Ter668Arg
ENST00000395105.8:c.2002T>C	ENSP00000378537.4:p.Ter668Arg
ENST00000416286.7:c.1978T>C	ENSP00000400403.3:p.Ter660Arg
ENST00000423167.6:c.1975T>C	ENSP00000413012.2:p.Ter659Arg
ENST00000449139.6:c.2002T>C	ENSP00000410221.2:p.Ter668Arg
ENST00000535552.5:c.2113T>C	ENSP00000440238.1:p.Ter705Arg
ENST00000545137.5:n.1711T>C
ENST00000563965.5:c.2119T>C	ENSP00000456609.1:p.Ter707Arg
ENST00000574278.5:c.2047T>C	ENSP00000458827.1:p.Ter683Arg
ENST00000574439.5:n.2274T>C
ENST00000616000.4:c.2002T>C	ENSP00000479112.1:p.Ter668Arg
NM_001142617.1:c.2002T>C	NP_001136089.1:p.Ter668Arg
NM_001142618.1:c.2002T>C	NP_001136090.1:p.Ter668Arg
NM_001142619.1:c.1975T>C	NP_001136091.1:p.Ter659Arg
NM_001199040.1:c.2113T>C	NP_001185969.1:p.Ter705Arg
NM_001199041.1:c.2047T>C	NP_001185970.1:p.Ter683Arg
NM_001199042.1:c.2119T>C	NP_001185971.1:p.Ter707Arg
NM_022369.3:c.2002T>C	NP_071764.3:p.Ter668Arg
XM_011521883.1:c.2002T>C	XP_011520185.1:p.Ter668Arg
XM_011521884.1:c.1813T>C	XP_011520186.1:p.Ter605Arg
XM_017022478.1:c.2050T>C	XP_016877967.1:p.Ter684Arg
XM_017022479.1:c.2002T>C	XP_016877968.1:p.Ter668Arg
XM_017022480.1:c.1813T>C	XP_016877969.1:p.Ter605Arg
NM_022369.4:c.2002T>C MANE Select	NP_071764.3:p.Ter668Arg
NM_001142617.2:c.2002T>C	NP_001136089.1:p.Ter668Arg
NM_001142619.2:c.1975T>C	NP_001136091.1:p.Ter659Arg
NM_001199042.2:c.2119T>C	NP_001185971.1:p.Ter707Arg
NM_001142618.2:c.2002T>C	NP_001136090.1:p.Ter668Arg
NM_001199040.2:c.2113T>C	NP_001185969.1:p.Ter705Arg
NM_001199041.2:c.2047T>C	NP_001185970.1:p.Ter683Arg