Canonical Allele Identifier: CA1593854547

Gene: SGCD

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.156754949_156754964delinsTTATTTCGGGAAGATA , CM000667.2:g.156754949_156754964delinsTTATTTCGGGAAGATA	GRCh38
NC_000005.9:g.156181960_156181975delinsTTATTTCGGGAAGATA , CM000667.1:g.156181960_156181975delinsTTATTTCGGGAAGATA	GRCh37
NC_000005.8:g.156114538_156114553delinsTTATTTCGGGAAGATA	NCBI36
NG_008693.2:g.889607_889622delinsTTATTTCGGGAAGATA , LRG_205:g.889607_889622delinsTTATTTCGGGAAGATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337851.9:c.576-2632_576-2617delinsTTATTTCGGGAAGATA MANE Select	ENSP00000338343.4:n.576-2632_576-2617delinsTTATTTCGGGAAGATA
ENST00000337851.8:c.576-2632_576-2617delinsTTATTTCGGGAAGATA	ENSP00000338343.4:n.576-2632_576-2617delinsTTATTTCGGGAAGATA
ENST00000435422.7:c.573-2632_573-2617delinsTTATTTCGGGAAGATA	ENSP00000403003.2:n.573-2632_573-2617delinsTTATTTCGGGAAGATA
ENST00000517913.5:c.576-2632_576-2617delinsTTATTTCGGGAAGATA	ENSP00000429378.1:n.576-2632_576-2617delinsTTATTTCGGGAAGATA
NM_000337.5:c.576-2632_576-2617delinsTTATTTCGGGAAGATA , LRG_205t1:c.576-2632_576-2617delinsTTATTTCGGGAAGATA	NP_000328.2:n.576-2632_576-2617delinsTTATTTCGGGAAGATA
NM_001128209.1:c.573-2632_573-2617delinsTTATTTCGGGAAGATA	NP_001121681.1:n.573-2632_573-2617delinsTTATTTCGGGAAGATA
NM_172244.2:c.576-2632_576-2617delinsTTATTTCGGGAAGATA	NP_758447.1:n.576-2632_576-2617delinsTTATTTCGGGAAGATA
XM_005265966.3:c.576-2632_576-2617delinsTTATTTCGGGAAGATA	XP_005266023.1:n.576-2632_576-2617delinsTTATTTCGGGAAGATA
XM_005265967.1:c.503-2632_503-2617delinsTTATTTCGGGAAGATA	XP_005266024.1:n.503-2632_503-2617delinsTTATTTCGGGAAGATA
XM_006714911.2:c.576-2632_576-2617delinsTTATTTCGGGAAGATA	XP_006714974.1:n.576-2632_576-2617delinsTTATTTCGGGAAGATA
XM_011534621.1:c.573-2632_573-2617delinsTTATTTCGGGAAGATA	XP_011532923.1:n.573-2632_573-2617delinsTTATTTCGGGAAGATA
XM_005265966.5:c.576-2632_576-2617delinsTTATTTCGGGAAGATA	XP_005266023.1:n.576-2632_576-2617delinsTTATTTCGGGAAGATA
XM_005265967.2:c.503-2632_503-2617delinsTTATTTCGGGAAGATA	XP_005266024.1:n.503-2632_503-2617delinsTTATTTCGGGAAGATA
XM_011534621.2:c.573-2632_573-2617delinsTTATTTCGGGAAGATA	XP_011532923.1:n.573-2632_573-2617delinsTTATTTCGGGAAGATA
XM_017009723.2:c.576-2632_576-2617delinsTTATTTCGGGAAGATA	XP_016865212.1:n.576-2632_576-2617delinsTTATTTCGGGAAGATA
XM_017009724.1:c.576-2632_576-2617delinsTTATTTCGGGAAGATA	XP_016865213.1:n.576-2632_576-2617delinsTTATTTCGGGAAGATA
NM_001128209.2:c.573-2632_573-2617delinsTTATTTCGGGAAGATA	NP_001121681.1:n.573-2632_573-2617delinsTTATTTCGGGAAGATA
NM_172244.3:c.576-2632_576-2617delinsTTATTTCGGGAAGATA	NP_758447.1:n.576-2632_576-2617delinsTTATTTCGGGAAGATA
NM_000337.6:c.576-2632_576-2617delinsTTATTTCGGGAAGATA MANE Select	NP_000328.2:n.576-2632_576-2617delinsTTATTTCGGGAAGATA