Canonical Allele Identifier: CA1335698078

Gene: SAG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233346799_233346800delinsTA , CM000664.2:g.233346799_233346800delinsTA	GRCh38
NC_000002.11:g.234255445_234255446delinsTA , CM000664.1:g.234255445_234255446delinsTA	GRCh37
NC_000002.10:g.233920184_233920185delinsTA	NCBI36
NG_009116.1:g.44137_44138delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409110.6:c.1113-8_1113-7delinsTA MANE Select	ENSP00000386444.1:n.1113-8_1113-7delinsTA
ENST00000409110.5:c.1113-8_1113-7delinsTA	ENSP00000386444.1:n.1113-8_1113-7delinsTA
ENST00000412969.6:n.2333-8_2333-7delinsTA
ENST00000471884.5:n.3144-8_3144-7delinsTA
ENST00000474220.5:n.319-8_319-7delinsTA
ENST00000476500.5:n.6412-8_6412-7delinsTA
ENST00000492629.1:n.74-8_74-7delinsTA
NM_000541.4:c.1113-8_1113-7delinsTA	NP_000532.2:n.1113-8_1113-7delinsTA
XM_011511589.1:c.1113-8_1113-7delinsTA	XP_011509891.1:n.1113-8_1113-7delinsTA
XM_011511590.1:c.1113-8_1113-7delinsTA	XP_011509892.1:n.1113-8_1113-7delinsTA
XM_011511591.1:c.1103-8_1103-7delinsTA	XP_011509893.1:n.1103-8_1103-7delinsTA
XM_011511592.1:c.957-8_957-7delinsTA	XP_011509894.1:n.957-8_957-7delinsTA
XM_011511593.1:c.813-8_813-7delinsTA	XP_011509895.1:n.813-8_813-7delinsTA
XM_011511594.1:c.741-8_741-7delinsTA	XP_011509896.1:n.741-8_741-7delinsTA
XM_011511596.1:c.711-8_711-7delinsTA	XP_011509898.1:n.711-8_711-7delinsTA
XM_011511597.1:c.711-8_711-7delinsTA	XP_011509899.1:n.711-8_711-7delinsTA
XR_922978.1:n.1430-8_1430-7delinsTA
XR_922979.1:n.1434-8_1434-7delinsTA
XR_922980.1:n.1529-8_1529-7delinsTA
XM_011511593.3:c.813-8_813-7delinsTA	XP_011509895.1:n.813-8_813-7delinsTA
XM_017004641.1:c.1103-8_1103-7delinsTA	XP_016860130.1:n.1103-8_1103-7delinsTA
XM_024453036.1:c.701-8_701-7delinsTA	XP_024308804.1:n.701-8_701-7delinsTA
XR_001738882.1:n.1311-8_1311-7delinsTA
XR_922980.2:n.1529-8_1529-7delinsTA
NM_000541.5:c.1113-8_1113-7delinsTA MANE Select	NP_000532.2:n.1113-8_1113-7delinsTA