Canonical Allele Identifier: CA1335698034
Gene: SAG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233346703_233346704delinsGA , CM000664.2:g.233346703_233346704delinsGA GRCh38
NC_000002.11:g.234255349_234255350delinsGA , CM000664.1:g.234255349_234255350delinsGA GRCh37
NC_000002.10:g.233920088_233920089delinsGA NCBI36
NG_009116.1:g.44041_44042delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000409110.6:c.1113-104_1113-103delinsGA MANE Select ENSP00000386444.1:n.1113-104_1113-103delinsGA
ENST00000409110.5:c.1113-104_1113-103delinsGA ENSP00000386444.1:n.1113-104_1113-103delinsGA
ENST00000412969.6:n.2333-104_2333-103delinsGA
ENST00000471884.5:n.3144-104_3144-103delinsGA
ENST00000474220.5:n.319-104_319-103delinsGA
ENST00000476500.5:n.6412-104_6412-103delinsGA
ENST00000492629.1:n.74-104_74-103delinsGA
NM_000541.4:c.1113-104_1113-103delinsGA NP_000532.2:n.1113-104_1113-103delinsGA
XM_011511589.1:c.1113-104_1113-103delinsGA XP_011509891.1:n.1113-104_1113-103delinsGA
XM_011511590.1:c.1113-104_1113-103delinsGA XP_011509892.1:n.1113-104_1113-103delinsGA
XM_011511591.1:c.1103-104_1103-103delinsGA XP_011509893.1:n.1103-104_1103-103delinsGA
XM_011511592.1:c.957-104_957-103delinsGA XP_011509894.1:n.957-104_957-103delinsGA
XM_011511593.1:c.813-104_813-103delinsGA XP_011509895.1:n.813-104_813-103delinsGA
XM_011511594.1:c.741-104_741-103delinsGA XP_011509896.1:n.741-104_741-103delinsGA
XM_011511596.1:c.711-104_711-103delinsGA XP_011509898.1:n.711-104_711-103delinsGA
XM_011511597.1:c.711-104_711-103delinsGA XP_011509899.1:n.711-104_711-103delinsGA
XR_922978.1:n.1430-104_1430-103delinsGA
XR_922979.1:n.1434-104_1434-103delinsGA
XR_922980.1:n.1529-104_1529-103delinsGA
XM_011511593.3:c.813-104_813-103delinsGA XP_011509895.1:n.813-104_813-103delinsGA
XM_017004641.1:c.1103-104_1103-103delinsGA XP_016860130.1:n.1103-104_1103-103delinsGA
XM_024453036.1:c.701-104_701-103delinsGA XP_024308804.1:n.701-104_701-103delinsGA
XR_001738882.1:n.1311-104_1311-103delinsGA
XR_922980.2:n.1529-104_1529-103delinsGA
NM_000541.5:c.1113-104_1113-103delinsGA MANE Select NP_000532.2:n.1113-104_1113-103delinsGA