Canonical Allele Identifier: CA2809770669

Gene: SGCA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50167811_50167812insGG , CM000679.2:g.50167811_50167812insGG	GRCh38
NC_000017.10:g.48245172_48245173insGG , CM000679.1:g.48245172_48245173insGG	GRCh37
NC_000017.9:g.45600171_45600172insGG	NCBI36
NG_008889.1:g.6807_6808insGG , LRG_203:g.6807_6808insGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504073.2:c.312+75_312+76insGG	ENSP00000422030.2:n.312+75_312+76insGG
ENST00000511303.6:n.38-136_38-135insGG
ENST00000512526.2:c.303+84_303+85insGG	ENSP00000426606.2:n.303+84_303+85insGG
ENST00000682109.1:c.192+75_192+76insGG	ENSP00000508041.1:n.192+75_192+76insGG
ENST00000683226.1:n.22+75_22+76insGG
ENST00000683294.1:c.312+75_312+76insGG	ENSP00000508134.1:n.312+75_312+76insGG
ENST00000262018.8:c.312+75_312+76insGG MANE Select	ENSP00000262018.3:n.312+75_312+76insGG
ENST00000262018.7:c.312+75_312+76insGG	ENSP00000262018.3:n.312+75_312+76insGG
ENST00000344627.10:c.312+75_312+76insGG	ENSP00000345522.6:n.312+75_312+76insGG
ENST00000502555.5:c.158-136_158-135insGG	ENSP00000422817.1:n.158-136_158-135insGG
ENST00000511303.5:c.34-136_34-135insGG	ENSP00000426104.1:n.34-136_34-135insGG
ENST00000512526.1:c.147+84_147+85insGG
ENST00000513821.5:c.312+75_312+76insGG	ENSP00000426571.1:n.312+75_312+76insGG
ENST00000513942.5:n.104-136_104-135insGG
ENST00000514934.1:c.*19-136_*19-135insGG	ENSP00000423168.1:n.*19-136_*19-135insGG
NM_000023.2:c.312+75_312+76insGG , LRG_203t1:c.312+75_312+76insGG	NP_000014.1:n.312+75_312+76insGG
NM_001135697.1:c.312+75_312+76insGG	NP_001129169.1:n.312+75_312+76insGG
XM_011525120.1:c.312+75_312+76insGG	XP_011523422.1:n.312+75_312+76insGG
XM_011525121.1:c.312+75_312+76insGG	XP_011523423.1:n.312+75_312+76insGG
XM_011525122.1:c.312+75_312+76insGG	XP_011523424.1:n.312+75_312+76insGG
XM_011525123.1:c.312+75_312+76insGG	XP_011523425.1:n.312+75_312+76insGG
XM_011525124.1:c.7-136_7-135insGG	XP_011523426.1:n.7-136_7-135insGG
XR_934517.1:n.378+75_378+76insGG
NM_000023.3:c.312+75_312+76insGG	NP_000014.1:n.312+75_312+76insGG
NM_001135697.2:c.312+75_312+76insGG	NP_001129169.1:n.312+75_312+76insGG
NR_135553.1:n.368+75_368+76insGG
XM_011525120.2:c.474+75_474+76insGG	XP_011523422.2:n.474+75_474+76insGG
XM_011525121.2:c.474+75_474+76insGG	XP_011523423.2:n.474+75_474+76insGG
XM_011525122.2:c.474+75_474+76insGG	XP_011523424.2:n.474+75_474+76insGG
XM_011525123.2:c.474+75_474+76insGG	XP_011523425.2:n.474+75_474+76insGG
XM_011525124.2:c.7-136_7-135insGG	XP_011523426.1:n.7-136_7-135insGG
XM_024450873.1:c.7-136_7-135insGG	XP_024306641.1:n.7-136_7-135insGG
XR_002958056.1:n.830+75_830+76insGG
NM_000023.4:c.312+75_312+76insGG MANE Select	NP_000014.1:n.312+75_312+76insGG
NM_001135697.3:c.312+75_312+76insGG	NP_001129169.1:n.312+75_312+76insGG
NR_135553.2:n.348+75_348+76insGG