Canonical Allele Identifier: CA2754682964

Gene: SAG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233346752_233346798del , CM000664.2:g.233346752_233346798del	GRCh38
NC_000002.11:g.234255398_234255444del , CM000664.1:g.234255398_234255444del	GRCh37
NC_000002.10:g.233920137_233920183del	NCBI36
NG_009116.1:g.44090_44136del

Transcript Alleles

HGVS	Amino-acid change
ENST00000409110.6:c.1113-55_1113-9del MANE Select	ENSP00000386444.1:n.1113-55_1113-9del
ENST00000409110.5:c.1113-55_1113-9del	ENSP00000386444.1:n.1113-55_1113-9del
ENST00000412969.6:n.2333-55_2333-9del
ENST00000471884.5:n.3144-55_3144-9del
ENST00000474220.5:n.319-55_319-9del
ENST00000476500.5:n.6412-55_6412-9del
ENST00000492629.1:n.74-55_74-9del
NM_000541.4:c.1113-55_1113-9del	NP_000532.2:n.1113-55_1113-9del
XM_011511589.1:c.1113-55_1113-9del	XP_011509891.1:n.1113-55_1113-9del
XM_011511590.1:c.1113-55_1113-9del	XP_011509892.1:n.1113-55_1113-9del
XM_011511591.1:c.1103-55_1103-9del	XP_011509893.1:n.1103-55_1103-9del
XM_011511592.1:c.957-55_957-9del	XP_011509894.1:n.957-55_957-9del
XM_011511593.1:c.813-55_813-9del	XP_011509895.1:n.813-55_813-9del
XM_011511594.1:c.741-55_741-9del	XP_011509896.1:n.741-55_741-9del
XM_011511596.1:c.711-55_711-9del	XP_011509898.1:n.711-55_711-9del
XM_011511597.1:c.711-55_711-9del	XP_011509899.1:n.711-55_711-9del
XR_922978.1:n.1430-55_1430-9del
XR_922979.1:n.1434-55_1434-9del
XR_922980.1:n.1529-55_1529-9del
XM_011511593.3:c.813-55_813-9del	XP_011509895.1:n.813-55_813-9del
XM_017004641.1:c.1103-55_1103-9del	XP_016860130.1:n.1103-55_1103-9del
XM_024453036.1:c.701-55_701-9del	XP_024308804.1:n.701-55_701-9del
XR_001738882.1:n.1311-55_1311-9del
XR_922980.2:n.1529-55_1529-9del
NM_000541.5:c.1113-55_1113-9del MANE Select	NP_000532.2:n.1113-55_1113-9del