Canonical Allele Identifier: CA491173214

Gene: STRA6

Linked Data

• MyVariant Identifiers: chr15:g.74483205T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74190864T>A , CM000677.2:g.74190864T>A	GRCh38
NC_000015.9:g.74483205T>A , CM000677.1:g.74483205T>A	GRCh37
NC_000015.8:g.72270258T>A	NCBI36
NG_009207.1:g.23167A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000395105.9:c.903A>T MANE Select	ENSP00000378537.4:p.Thr301=
ENST00000323940.9:c.903A>T	ENSP00000326085.5:p.Thr301=
ENST00000395105.8:c.903A>T	ENSP00000378537.4:p.Thr301=
ENST00000416286.7:c.879A>T	ENSP00000400403.3:p.Thr293=
ENST00000423167.6:c.876A>T	ENSP00000413012.2:p.Thr292=
ENST00000449139.6:c.903A>T	ENSP00000410221.2:p.Thr301=
ENST00000535552.5:c.1014A>T	ENSP00000440238.1:p.Thr338=
ENST00000545137.5:n.612A>T
ENST00000563965.5:c.1020A>T	ENSP00000456609.1:p.Thr340=
ENST00000569936.5:c.1033A>T	ENSP00000461799.1:p.Thr345Ser
ENST00000574278.5:c.948A>T	ENSP00000458827.1:p.Thr316=
ENST00000574439.5:n.1175A>T
ENST00000616000.4:c.903A>T	ENSP00000479112.1:p.Thr301=
NM_001142617.1:c.903A>T	NP_001136089.1:p.Thr301=
NM_001142618.1:c.903A>T	NP_001136090.1:p.Thr301=
NM_001142619.1:c.876A>T	NP_001136091.1:p.Thr292=
NM_001199040.1:c.1014A>T	NP_001185969.1:p.Thr338=
NM_001199041.1:c.948A>T	NP_001185970.1:p.Thr316=
NM_001199042.1:c.1020A>T	NP_001185971.1:p.Thr340=
NM_022369.3:c.903A>T	NP_071764.3:p.Thr301=
XM_011521883.1:c.903A>T	XP_011520185.1:p.Thr301=
XM_011521884.1:c.714A>T	XP_011520186.1:p.Thr238=
XM_011521885.1:c.1020A>T	XP_011520187.1:p.Thr340=
XR_931877.1:n.1026A>T
XM_011521885.2:c.1020A>T	XP_011520187.1:p.Thr340=
XM_017022478.1:c.951A>T	XP_016877967.1:p.Thr317=
XM_017022479.1:c.903A>T	XP_016877968.1:p.Thr301=
XM_017022480.1:c.714A>T	XP_016877969.1:p.Thr238=
XR_931877.2:n.1026A>T
NM_022369.4:c.903A>T MANE Select	NP_071764.3:p.Thr301=
NM_001142617.2:c.903A>T	NP_001136089.1:p.Thr301=
NM_001142619.2:c.876A>T	NP_001136091.1:p.Thr292=
NM_001199042.2:c.1020A>T	NP_001185971.1:p.Thr340=
NM_001142618.2:c.903A>T	NP_001136090.1:p.Thr301=
NM_001199040.2:c.1014A>T	NP_001185969.1:p.Thr338=
NM_001199041.2:c.948A>T	NP_001185970.1:p.Thr316=