Canonical Allele Identifier: CA2263905219

Gene: SGCA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50167764_50167766delinsCAG , CM000679.2:g.50167764_50167766delinsCAG	GRCh38
NC_000017.10:g.48245125_48245127delinsCAG , CM000679.1:g.48245125_48245127delinsCAG	GRCh37
NC_000017.9:g.45600124_45600126delinsCAG	NCBI36
NG_008889.1:g.6760_6762delinsCAG , LRG_203:g.6760_6762delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504073.2:c.312+28_312+30delinsCAG	ENSP00000422030.2:n.312+28_312+30delinsCAG
ENST00000511303.6:n.38-183_38-181delinsCAG
ENST00000512526.2:c.303+37_303+39delinsCAG	ENSP00000426606.2:n.303+37_303+39delinsCAG
ENST00000682109.1:c.192+28_192+30delinsCAG	ENSP00000508041.1:n.192+28_192+30delinsCAG
ENST00000683226.1:n.22+28_22+30delinsCAG
ENST00000683294.1:c.312+28_312+30delinsCAG	ENSP00000508134.1:n.312+28_312+30delinsCAG
ENST00000262018.8:c.312+28_312+30delinsCAG MANE Select	ENSP00000262018.3:n.312+28_312+30delinsCAG
ENST00000262018.7:c.312+28_312+30delinsCAG	ENSP00000262018.3:n.312+28_312+30delinsCAG
ENST00000344627.10:c.312+28_312+30delinsCAG	ENSP00000345522.6:n.312+28_312+30delinsCAG
ENST00000502555.5:c.158-183_158-181delinsCAG	ENSP00000422817.1:n.158-183_158-181delinsCAG
ENST00000511303.5:c.34-183_34-181delinsCAG	ENSP00000426104.1:n.34-183_34-181delinsCAG
ENST00000512526.1:c.147+37_147+39delinsCAG
ENST00000513821.5:c.312+28_312+30delinsCAG	ENSP00000426571.1:n.312+28_312+30delinsCAG
ENST00000513942.5:n.104-183_104-181delinsCAG
ENST00000514934.1:c.*19-183_*19-181delinsCAG	ENSP00000423168.1:n.*19-183_*19-181delinsCAG
NM_000023.2:c.312+28_312+30delinsCAG , LRG_203t1:c.312+28_312+30delinsCAG	NP_000014.1:n.312+28_312+30delinsCAG
NM_001135697.1:c.312+28_312+30delinsCAG	NP_001129169.1:n.312+28_312+30delinsCAG
XM_011525120.1:c.312+28_312+30delinsCAG	XP_011523422.1:n.312+28_312+30delinsCAG
XM_011525121.1:c.312+28_312+30delinsCAG	XP_011523423.1:n.312+28_312+30delinsCAG
XM_011525122.1:c.312+28_312+30delinsCAG	XP_011523424.1:n.312+28_312+30delinsCAG
XM_011525123.1:c.312+28_312+30delinsCAG	XP_011523425.1:n.312+28_312+30delinsCAG
XM_011525124.1:c.7-183_7-181delinsCAG	XP_011523426.1:n.7-183_7-181delinsCAG
XR_934517.1:n.378+28_378+30delinsCAG
NM_000023.3:c.312+28_312+30delinsCAG	NP_000014.1:n.312+28_312+30delinsCAG
NM_001135697.2:c.312+28_312+30delinsCAG	NP_001129169.1:n.312+28_312+30delinsCAG
NR_135553.1:n.368+28_368+30delinsCAG
XM_011525120.2:c.474+28_474+30delinsCAG	XP_011523422.2:n.474+28_474+30delinsCAG
XM_011525121.2:c.474+28_474+30delinsCAG	XP_011523423.2:n.474+28_474+30delinsCAG
XM_011525122.2:c.474+28_474+30delinsCAG	XP_011523424.2:n.474+28_474+30delinsCAG
XM_011525123.2:c.474+28_474+30delinsCAG	XP_011523425.2:n.474+28_474+30delinsCAG
XM_011525124.2:c.7-183_7-181delinsCAG	XP_011523426.1:n.7-183_7-181delinsCAG
XM_024450873.1:c.7-183_7-181delinsCAG	XP_024306641.1:n.7-183_7-181delinsCAG
XR_002958056.1:n.830+28_830+30delinsCAG
NM_000023.4:c.312+28_312+30delinsCAG MANE Select	NP_000014.1:n.312+28_312+30delinsCAG
NM_001135697.3:c.312+28_312+30delinsCAG	NP_001129169.1:n.312+28_312+30delinsCAG
NR_135553.2:n.348+28_348+30delinsCAG