Canonical Allele Identifier: CA1483756

Gene: SDCCAG8

Linked Data

• dbSNP Id: rs760980526
• ExAC: 1:243589686 TA / T
• gnomAD v2: 1-243589686-TA-T
• MyVariant Identifiers: chr1:g.243589687del (hg19) ; chr1:g.243426385del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.243426386del , CM000663.2:g.243426386del	GRCh38
NC_000001.10:g.243589688del , CM000663.1:g.243589688del	GRCh37
NC_000001.9:g.241656311del	NCBI36
NG_027811.1:g.175382del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366541.8:c.1854-41del MANE Select	ENSP00000355499.3:n.1854-41del
ENST00000366541.7:c.1854-41del	ENSP00000355499.3:n.1854-41del
ENST00000435549.1:c.957-41del	ENSP00000410200.1:n.957-41del
ENST00000463042.1:n.61-41del
NM_006642.3:c.1854-41del	NP_006633.1:n.1854-41del
XM_005273013.3:c.1725-41del	XP_005273070.1:n.1725-41del
XM_005273018.1:c.1431-41del	XP_005273075.1:n.1431-41del
XM_005273021.3:c.951-41del	XP_005273078.1:n.951-41del
XM_005273022.2:c.933-41del	XP_005273079.1:n.933-41del
XM_006711727.2:c.1884-41del	XP_006711790.1:n.1884-41del
XM_006711728.2:c.1755-41del	XP_006711791.1:n.1755-41del
XM_006711729.2:c.1695-41del	XP_006711792.1:n.1695-41del
XM_011544021.1:c.1980-41del	XP_011542323.1:n.1980-41del
XM_011544022.1:c.1950-41del	XP_011542324.1:n.1950-41del
XM_011544023.1:c.1980-41del	XP_011542325.1:n.1980-41del
XM_011544024.1:c.1980-41del	XP_011542326.1:n.1980-41del
XM_011544025.1:c.1791-41del	XP_011542327.1:n.1791-41del
XM_011544026.1:c.1743-41del	XP_011542328.1:n.1743-41del
XM_011544027.1:c.1566-41del	XP_011542329.1:n.1566-41del
XM_011544028.1:c.1518-41del	XP_011542330.1:n.1518-41del
XM_011544030.1:c.909-41del	XP_011542332.1:n.909-41del
XR_949128.1:n.2004-41del
NM_001350246.1:c.951-41del	NP_001337175.1:n.951-41del
NM_001350247.1:c.951-41del	NP_001337176.1:n.951-41del
NM_001350248.1:c.1950-41del	NP_001337177.1:n.1950-41del
NM_001350249.1:c.1560-41del	NP_001337178.1:n.1560-41del
NM_001350251.1:c.951-41del	NP_001337180.1:n.951-41del
NM_006642.4:c.1854-41del	NP_006633.1:n.1854-41del
XM_005273013.5:c.1725-41del	XP_005273070.1:n.1725-41del
XM_005273018.2:c.1431-41del	XP_005273075.1:n.1431-41del
XM_005273022.4:c.933-41del	XP_005273079.1:n.933-41del
XM_011544026.3:c.1743-41del	XP_011542328.1:n.1743-41del
XM_011544028.3:c.1518-41del	XP_011542330.1:n.1518-41del
XM_011544030.3:c.909-41del	XP_011542332.1:n.909-41del
XM_017000104.2:c.1725-41del	XP_016855593.1:n.1725-41del
XM_017000105.2:c.1617-41del	XP_016855594.1:n.1617-41del
XM_024452537.1:c.1656-41del	XP_024308305.1:n.1656-41del
XM_024452539.1:c.1656-41del	XP_024308307.1:n.1656-41del
XM_024452540.1:c.1656-41del	XP_024308308.1:n.1656-41del
XM_024452547.1:c.1560-41del	XP_024308315.1:n.1560-41del
XM_024452548.1:c.1656-41del	XP_024308316.1:n.1656-41del
XM_024452549.1:c.1323-41del	XP_024308317.1:n.1323-41del
XR_002958955.1:n.1896-41del
XR_002958956.1:n.1896-41del
XR_002958965.1:n.1787-41del
NM_006642.5:c.1854-41del MANE Select	NP_006633.1:n.1854-41del
NM_001350246.2:c.951-41del	NP_001337175.1:n.951-41del
NM_001350247.2:c.951-41del	NP_001337176.1:n.951-41del
NM_001350248.2:c.1950-41del	NP_001337177.1:n.1950-41del
NM_001350249.2:c.1560-41del	NP_001337178.1:n.1560-41del
NM_001350251.2:c.951-41del	NP_001337180.1:n.951-41del