Canonical Allele Identifier: CA2187554595

Gene: STRA6

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74190762_74190763delinsTG , CM000677.2:g.74190762_74190763delinsTG	GRCh38
NC_000015.9:g.74483103_74483104delinsTG , CM000677.1:g.74483103_74483104delinsTG	GRCh37
NC_000015.8:g.72270156_72270157delinsTG	NCBI36
NG_009207.1:g.23268_23269delinsCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000395105.9:c.927+77_927+78delinsCA MANE Select	ENSP00000378537.4:n.927+77_927+78delinsCA...
ENST00000323940.9:c.927+77_927+78delinsCA	ENSP00000326085.5:n.927+77_927+78delinsCA...
ENST00000395105.8:c.927+77_927+78delinsCA	ENSP00000378537.4:n.927+77_927+78delinsCA...
ENST00000416286.7:c.903+77_903+78delinsCA	ENSP00000400403.3:n.903+77_903+78delinsCA...
ENST00000423167.6:c.900+77_900+78delinsCA	ENSP00000413012.2:n.900+77_900+78delinsCA...
ENST00000449139.6:c.927+77_927+78delinsCA	ENSP00000410221.2:n.927+77_927+78delinsCA...
ENST00000535552.5:c.1038+77_1038+78delinsCA	ENSP00000440238.1:n.1038+77_1038+78delins...
ENST00000545137.5:n.636+77_636+78delinsCA
ENST00000563965.5:c.1044+77_1044+78delinsCA	ENSP00000456609.1:n.1044+77_1044+78delins...
ENST00000569936.5:c.1057+77_1057+78delinsCA	ENSP00000461799.1:n.1057+77_1057+78delins...
ENST00000574278.5:c.972+77_972+78delinsCA	ENSP00000458827.1:n.972+77_972+78delinsCA...
ENST00000574439.5:n.1199+77_1199+78delinsCA
ENST00000616000.4:c.927+77_927+78delinsCA	ENSP00000479112.1:n.927+77_927+78delinsCA...
NM_001142617.1:c.927+77_927+78delinsCA	NP_001136089.1:n.927+77_927+78delinsCA
NM_001142618.1:c.927+77_927+78delinsCA	NP_001136090.1:n.927+77_927+78delinsCA
NM_001142619.1:c.900+77_900+78delinsCA	NP_001136091.1:n.900+77_900+78delinsCA
NM_001199040.1:c.1038+77_1038+78delinsCA	NP_001185969.1:n.1038+77_1038+78delinsCA
NM_001199041.1:c.972+77_972+78delinsCA	NP_001185970.1:n.972+77_972+78delinsCA
NM_001199042.1:c.1044+77_1044+78delinsCA	NP_001185971.1:n.1044+77_1044+78delinsCA
NM_022369.3:c.927+77_927+78delinsCA	NP_071764.3:n.927+77_927+78delinsCA
XM_011521883.1:c.927+77_927+78delinsCA	XP_011520185.1:n.927+77_927+78delinsCA
XM_011521884.1:c.738+77_738+78delinsCA	XP_011520186.1:n.738+77_738+78delinsCA
XM_011521885.1:c.1044+77_1044+78delinsCA	XP_011520187.1:n.1044+77_1044+78delinsCA
XR_931877.1:n.1050+77_1050+78delinsCA
XM_011521885.2:c.1044+77_1044+78delinsCA	XP_011520187.1:n.1044+77_1044+78delinsCA
XM_017022478.1:c.975+77_975+78delinsCA	XP_016877967.1:n.975+77_975+78delinsCA
XM_017022479.1:c.927+77_927+78delinsCA	XP_016877968.1:n.927+77_927+78delinsCA
XM_017022480.1:c.738+77_738+78delinsCA	XP_016877969.1:n.738+77_738+78delinsCA
XR_931877.2:n.1050+77_1050+78delinsCA
NM_022369.4:c.927+77_927+78delinsCA MANE Select	NP_071764.3:n.927+77_927+78delinsCA
NM_001142617.2:c.927+77_927+78delinsCA	NP_001136089.1:n.927+77_927+78delinsCA
NM_001142619.2:c.900+77_900+78delinsCA	NP_001136091.1:n.900+77_900+78delinsCA
NM_001199042.2:c.1044+77_1044+78delinsCA	NP_001185971.1:n.1044+77_1044+78delinsCA
NM_001142618.2:c.927+77_927+78delinsCA	NP_001136090.1:n.927+77_927+78delinsCA
NM_001199040.2:c.1038+77_1038+78delinsCA	NP_001185969.1:n.1038+77_1038+78delinsCA
NM_001199041.2:c.972+77_972+78delinsCA	NP_001185970.1:n.972+77_972+78delinsCA