Canonical Allele Identifier: CA345478185

Gene: SDCCAG8

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.243256219C>T , CM000663.2:g.243256219C>T	GRCh38
NC_000001.10:g.243419521C>T , CM000663.1:g.243419521C>T	GRCh37
NC_000001.9:g.241486144C>T	NCBI36
NG_027811.1:g.5215C>T
NG_029663.1:g.4188G>A
NG_029663.2:g.4188G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_006642.5:c.46C>T MANE Select	NP_006633.1:p.Gln16Ter
ENST00000366541.8:c.46C>T MANE Select	ENSP00000355499.3:p.Gln16Ter
NM_001350246.1:c.-1067C>T	NP_001337175.1:n.-1067C>T
NM_001350246.2:c.-1067C>T	NP_001337175.1:n.-1067C>T
NM_001350247.1:c.-955C>T	NP_001337176.1:n.-955C>T
NM_001350247.2:c.-955C>T	NP_001337176.1:n.-955C>T
NM_001350248.1:c.46C>T	NP_001337177.1:p.Gln16Ter
NM_001350248.2:c.46C>T	NP_001337177.1:p.Gln16Ter
NM_001350249.1:c.-262C>T	NP_001337178.1:n.-262C>T
NM_001350249.2:c.-262C>T	NP_001337178.1:n.-262C>T
NM_001350251.1:c.-1328C>T	NP_001337180.1:n.-1328C>T
NM_001350251.2:c.-1328C>T	NP_001337180.1:n.-1328C>T
NM_006642.3:c.46C>T	NP_006633.1:p.Gln16Ter
NM_006642.4:c.46C>T	NP_006633.1:p.Gln16Ter
ENST00000366541.7:c.46C>T	ENSP00000355499.3:p.Gln16Ter
ENST00000490065.5:n.186C>T
XM_005273013.3:c.46C>T	XP_005273070.1:p.Gln16Ter
XM_005273013.5:c.46C>T	XP_005273070.1:p.Gln16Ter
XM_005273018.1:c.-262C>T	XP_005273075.1:n.-262C>T
XM_005273018.2:c.-262C>T	XP_005273075.1:n.-262C>T
XM_005273022.2:c.-493C>T	XP_005273079.1:n.-493C>T
XM_005273022.4:c.-493C>T	XP_005273079.1:n.-493C>T
XM_005273023.3:c.46C>T	XP_005273080.1:p.Gln16Ter
XM_005273023.5:c.46C>T	XP_005273080.1:p.Gln16Ter
XM_006711727.2:c.84+693C>T	XP_006711790.1:n.84+693C>T
XM_006711728.2:c.84+693C>T	XP_006711791.1:n.84+693C>T
XM_006711729.2:c.84+693C>T	XP_006711792.1:n.84+693C>T
XM_011544021.1:c.84+693C>T	XP_011542323.1:n.84+693C>T
XM_011544022.1:c.46C>T	XP_011542324.1:p.Gln16Ter
XM_011544023.1:c.84+693C>T	XP_011542325.1:n.84+693C>T
XM_011544024.1:c.84+693C>T	XP_011542326.1:n.84+693C>T
XM_011544025.1:c.84+693C>T	XP_011542327.1:n.84+693C>T
XM_011544026.1:c.84+693C>T	XP_011542328.1:n.84+693C>T
XM_011544026.3:c.84+693C>T	XP_011542328.1:n.84+693C>T
XM_011544027.1:c.84+693C>T	XP_011542329.1:n.84+693C>T
XM_011544028.1:c.84+693C>T	XP_011542330.1:n.84+693C>T
XM_011544028.3:c.84+693C>T	XP_011542330.1:n.84+693C>T
XM_011544029.1:c.84+693C>T	XP_011542331.1:n.84+693C>T
XM_017000104.2:c.46C>T	XP_016855593.1:p.Gln16Ter
XM_017000105.2:c.46C>T	XP_016855594.1:p.Gln16Ter
XM_024452540.1:c.-262C>T	XP_024308308.1:n.-262C>T
XM_024452547.1:c.-262C>T	XP_024308315.1:n.-262C>T
XM_024452548.1:c.-228+693C>T	XP_024308316.1:n.-228+693C>T
XM_024452549.1:c.-262C>T	XP_024308317.1:n.-262C>T
XR_949128.1:n.108+693C>T