Canonical Allele Identifier: CA1483651
Community Standard Title: NM_006642.5(SDCCAG8):c.1473+48dup
Gene: SDCCAG8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.243344379dup , CM000663.2:g.243344379dup GRCh38
NC_000001.10:g.243507681dup , CM000663.1:g.243507681dup GRCh37
NC_000001.9:g.241574304dup NCBI36
NG_027811.1:g.93375dup

Transcript Alleles

HGVS Amino-acid Change
NM_006642.5:c.1473+48dup MANE Select NP_006633.1:n.1473+48dup
ENST00000366541.8:c.1473+48dup MANE Select ENSP00000355499.3:n.1473+48dup
NM_001350246.1:c.570+48dup NP_001337175.1:n.570+48dup
NM_001350246.2:c.570+48dup NP_001337175.1:n.570+48dup
NM_001350247.1:c.570+48dup NP_001337176.1:n.570+48dup
NM_001350247.2:c.570+48dup NP_001337176.1:n.570+48dup
NM_001350248.1:c.1569+48dup NP_001337177.1:n.1569+48dup
NM_001350248.2:c.1569+48dup NP_001337177.1:n.1569+48dup
NM_001350249.1:c.1179+48dup NP_001337178.1:n.1179+48dup
NM_001350249.2:c.1179+48dup NP_001337178.1:n.1179+48dup
NM_001350251.1:c.570+48dup NP_001337180.1:n.570+48dup
NM_001350251.2:c.570+48dup NP_001337180.1:n.570+48dup
NM_006642.3:c.1473+48dup NP_006633.1:n.1473+48dup
NM_006642.4:c.1473+48dup NP_006633.1:n.1473+48dup
ENST00000366541.7:c.1473+48dup ENSP00000355499.3:n.1473+48dup
ENST00000435549.1:c.813+48dup ENSP00000410200.1:n.813+48dup
ENST00000493334.1:n.440+48dup
XM_005273013.3:c.1344+48dup XP_005273070.1:n.1344+48dup
XM_005273013.5:c.1344+48dup XP_005273070.1:n.1344+48dup
XM_005273018.1:c.1050+48dup XP_005273075.1:n.1050+48dup
XM_005273018.2:c.1050+48dup XP_005273075.1:n.1050+48dup
XM_005273021.3:c.570+48dup XP_005273078.1:n.570+48dup
XM_005273022.2:c.552+48dup XP_005273079.1:n.552+48dup
XM_005273022.4:c.552+48dup XP_005273079.1:n.552+48dup
XM_006711727.2:c.1503+48dup XP_006711790.1:n.1503+48dup
XM_006711728.2:c.1374+48dup XP_006711791.1:n.1374+48dup
XM_006711729.2:c.1314+48dup XP_006711792.1:n.1314+48dup
XM_011544021.1:c.1599+48dup XP_011542323.1:n.1599+48dup
XM_011544022.1:c.1569+48dup XP_011542324.1:n.1569+48dup
XM_011544023.1:c.1599+48dup XP_011542325.1:n.1599+48dup
XM_011544024.1:c.1599+48dup XP_011542326.1:n.1599+48dup
XM_011544025.1:c.1410+48dup XP_011542327.1:n.1410+48dup
XM_011544026.1:c.1599+48dup XP_011542328.1:n.1599+48dup
XM_011544026.3:c.1599+48dup XP_011542328.1:n.1599+48dup
XM_011544027.1:c.1185+48dup XP_011542329.1:n.1185+48dup
XM_011544028.1:c.1374+48dup XP_011542330.1:n.1374+48dup
XM_011544028.3:c.1374+48dup XP_011542330.1:n.1374+48dup
XM_011544030.1:c.528+48dup XP_011542332.1:n.528+48dup
XM_011544030.3:c.528+48dup XP_011542332.1:n.528+48dup
XM_017000104.2:c.1344+48dup XP_016855593.1:n.1344+48dup
XM_017000105.2:c.1473+48dup XP_016855594.1:n.1473+48dup
XM_024452537.1:c.1275+48dup XP_024308305.1:n.1275+48dup
XM_024452539.1:c.1275+48dup XP_024308307.1:n.1275+48dup
XM_024452540.1:c.1275+48dup XP_024308308.1:n.1275+48dup
XM_024452547.1:c.1179+48dup XP_024308315.1:n.1179+48dup
XM_024452548.1:c.1275+48dup XP_024308316.1:n.1275+48dup
XM_024452549.1:c.1179+48dup XP_024308317.1:n.1179+48dup
XR_002958955.1:n.1515+48dup
XR_002958956.1:n.1515+48dup
XR_002958965.1:n.1515+48dup
XR_949128.1:n.1623+48dup