Canonical Allele Identifier: CA1335698086

Gene: SAG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233346816_233346826delinsTGCAAATTTAG , CM000664.2:g.233346816_233346826delinsTGCAAATTTAG	GRCh38
NC_000002.11:g.234255462_234255472delinsTGCAAATTTAG , CM000664.1:g.234255462_234255472delinsTGCAAATTTAG	GRCh37
NC_000002.10:g.233920201_233920211delinsTGCAAATTTAG	NCBI36
NG_009116.1:g.44154_44164delinsTGCAAATTTAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409110.6:c.1122_1132delinsTGCAAATTTAG MANE Select	ENSP00000386444.1:p.Asp374=
ENST00000409110.5:c.1122_1132delinsTGCAAATTTAG	ENSP00000386444.1:p.Asp374=
ENST00000412969.6:n.2342_2352delinsTGCAAATTTAG
ENST00000471884.5:n.3153_3163delinsTGCAAATTTAG
ENST00000474220.5:n.328_338delinsTGCAAATTTAG
ENST00000476500.5:n.6421_6431delinsTGCAAATTTAG
ENST00000492629.1:n.83_93delinsTGCAAATTTAG
NM_000541.4:c.1122_1132delinsTGCAAATTTAG	NP_000532.2:p.Asp374=
XM_011511589.1:c.1122_1132delinsTGCAAATTTAG	XP_011509891.1:p.Asp374=
XM_011511590.1:c.1122_1132delinsTGCAAATTTAG	XP_011509892.1:p.Asp374=
XM_011511591.1:c.1112_1122delinsTGCAAATTTAG	XP_011509893.1:p.Met371=
XM_011511592.1:c.966_976delinsTGCAAATTTAG	XP_011509894.1:p.Asp322=
XM_011511593.1:c.822_832delinsTGCAAATTTAG	XP_011509895.1:p.Asp274=
XM_011511594.1:c.750_760delinsTGCAAATTTAG	XP_011509896.1:p.Asp250=
XM_011511596.1:c.720_730delinsTGCAAATTTAG	XP_011509898.1:p.Asp240=
XM_011511597.1:c.720_730delinsTGCAAATTTAG	XP_011509899.1:p.Asp240=
XR_922978.1:n.1439_1449delinsTGCAAATTTAG
XR_922979.1:n.1443_1453delinsTGCAAATTTAG
XR_922980.1:n.1538_1548delinsTGCAAATTTAG
XM_011511593.3:c.822_832delinsTGCAAATTTAG	XP_011509895.1:p.Asp274=
XM_017004641.1:c.1112_1122delinsTGCAAATTTAG	XP_016860130.1:p.Met371=
XM_024453036.1:c.710_720delinsTGCAAATTTAG	XP_024308804.1:p.Met237=
XR_001738882.1:n.1320_1330delinsTGCAAATTTAG
XR_922980.2:n.1538_1548delinsTGCAAATTTAG
NM_000541.5:c.1122_1132delinsTGCAAATTTAG MANE Select	NP_000532.2:p.Asp374=