Canonical Allele Identifier: CA2263905037

Gene: SGCA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50167212_50167213delinsTC , CM000679.2:g.50167212_50167213delinsTC	GRCh38
NC_000017.10:g.48244573_48244574delinsTC , CM000679.1:g.48244573_48244574delinsTC	GRCh37
NC_000017.9:g.45599572_45599573delinsTC	NCBI36
NG_008889.1:g.6208_6209delinsTC , LRG_203:g.6208_6209delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504073.2:c.38-156_38-155delinsTC	ENSP00000422030.2:n.38-156_38-155delinsTC
ENST00000511303.6:n.38-735_38-734delinsTC
ENST00000512526.2:c.38-156_38-155delinsTC	ENSP00000426606.2:n.38-156_38-155delinsTC
ENST00000682109.1:c.38-370_38-369delinsTC	ENSP00000508041.1:n.38-370_38-369delinsTC
ENST00000683294.1:c.38-156_38-155delinsTC	ENSP00000508134.1:n.38-156_38-155delinsTC
ENST00000262018.8:c.38-156_38-155delinsTC MANE Select	ENSP00000262018.3:n.38-156_38-155delinsTC
ENST00000262018.7:c.38-156_38-155delinsTC	ENSP00000262018.3:n.38-156_38-155delinsTC
ENST00000344627.10:c.38-156_38-155delinsTC	ENSP00000345522.6:n.38-156_38-155delinsTC
ENST00000502555.5:c.38-156_38-155delinsTC	ENSP00000422817.1:n.38-156_38-155delinsTC
ENST00000511303.5:c.34-735_34-734delinsTC	ENSP00000426104.1:n.34-735_34-734delinsTC
ENST00000513821.5:c.38-156_38-155delinsTC	ENSP00000426571.1:n.38-156_38-155delinsTC
ENST00000513942.5:n.104-735_104-734delinsTC
ENST00000514934.1:c.97-156_97-155delinsTC	ENSP00000423168.1:n.97-156_97-155delinsTC
NM_000023.2:c.38-156_38-155delinsTC , LRG_203t1:c.38-156_38-155delinsTC	NP_000014.1:n.38-156_38-155delinsTC
NM_001135697.1:c.38-156_38-155delinsTC	NP_001129169.1:n.38-156_38-155delinsTC
XM_011525120.1:c.38-156_38-155delinsTC	XP_011523422.1:n.38-156_38-155delinsTC
XM_011525121.1:c.38-156_38-155delinsTC	XP_011523423.1:n.38-156_38-155delinsTC
XM_011525122.1:c.38-156_38-155delinsTC	XP_011523424.1:n.38-156_38-155delinsTC
XM_011525123.1:c.38-156_38-155delinsTC	XP_011523425.1:n.38-156_38-155delinsTC
XM_011525124.1:c.-114-156_-114-155delinsTC	XP_011523426.1:n.-114-156_-114-155delinsTC
XR_934517.1:n.104-156_104-155delinsTC
NM_000023.3:c.38-156_38-155delinsTC	NP_000014.1:n.38-156_38-155delinsTC
NM_001135697.2:c.38-156_38-155delinsTC	NP_001129169.1:n.38-156_38-155delinsTC
NR_135553.1:n.94-156_94-155delinsTC
XM_011525120.2:c.200-156_200-155delinsTC	XP_011523422.2:n.200-156_200-155delinsTC
XM_011525121.2:c.200-156_200-155delinsTC	XP_011523423.2:n.200-156_200-155delinsTC
XM_011525122.2:c.200-156_200-155delinsTC	XP_011523424.2:n.200-156_200-155delinsTC
XM_011525123.2:c.200-156_200-155delinsTC	XP_011523425.2:n.200-156_200-155delinsTC
XM_011525124.2:c.-114-156_-114-155delinsTC	XP_011523426.1:n.-114-156_-114-155delinsTC
XM_024450873.1:c.-114-156_-114-155delinsTC	XP_024306641.1:n.-114-156_-114-155delinsTC
XR_002958056.1:n.556-156_556-155delinsTC
NM_000023.4:c.38-156_38-155delinsTC MANE Select	NP_000014.1:n.38-156_38-155delinsTC
NM_001135697.3:c.38-156_38-155delinsTC	NP_001129169.1:n.38-156_38-155delinsTC
NR_135553.2:n.74-156_74-155delinsTC