Canonical Allele Identifier: CA2638704446
Gene: SGCA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50168278del , CM000679.2:g.50168278del GRCh38
NC_000017.10:g.48245639del , CM000679.1:g.48245639del GRCh37
NC_000017.9:g.45600638del NCBI36
NG_008889.1:g.7274del , LRG_203:g.7274del

Transcript Alleles

HGVS Amino-acid change
ENST00000504073.2:c.386-96del ENSP00000422030.2:n.386-96del
ENST00000511303.6:n.111-96del
ENST00000512526.2:c.377-96del ENSP00000426606.2:n.377-96del
ENST00000682109.1:c.266-96del ENSP00000508041.1:n.266-96del
ENST00000683226.1:n.96-96del
ENST00000683294.1:c.386-96del ENSP00000508134.1:n.386-96del
ENST00000262018.8:c.386-96del MANE Select ENSP00000262018.3:n.386-96del
ENST00000262018.7:c.386-96del ENSP00000262018.3:n.386-96del
ENST00000344627.10:c.386-96del ENSP00000345522.6:n.386-96del
ENST00000502555.5:c.*45-96del ENSP00000422817.1:n.*45-96del
ENST00000511303.5:c.107-96del ENSP00000426104.1:n.107-96del
ENST00000512526.1:c.221-96del
ENST00000513821.5:c.386-96del ENSP00000426571.1:n.386-96del
ENST00000513942.5:n.177-96del
ENST00000514934.1:c.*92-96del ENSP00000423168.1:n.*92-96del
NM_000023.2:c.386-96del , LRG_203t1:c.386-96del NP_000014.1:n.386-96del
NM_001135697.1:c.386-96del NP_001129169.1:n.386-96del
XM_011525120.1:c.386-96del XP_011523422.1:n.386-96del
XM_011525121.1:c.386-96del XP_011523423.1:n.386-96del
XM_011525122.1:c.386-96del XP_011523424.1:n.386-96del
XM_011525123.1:c.386-96del XP_011523425.1:n.386-96del
XM_011525124.1:c.80-96del XP_011523426.1:n.80-96del
XR_934517.1:n.452-96del
NM_000023.3:c.386-96del NP_000014.1:n.386-96del
NM_001135697.2:c.386-96del NP_001129169.1:n.386-96del
NR_135553.1:n.442-96del
XM_011525120.2:c.548-96del XP_011523422.2:n.548-96del
XM_011525121.2:c.548-96del XP_011523423.2:n.548-96del
XM_011525122.2:c.548-96del XP_011523424.2:n.548-96del
XM_011525123.2:c.548-96del XP_011523425.2:n.548-96del
XM_011525124.2:c.80-96del XP_011523426.1:n.80-96del
XM_024450873.1:c.80-96del XP_024306641.1:n.80-96del
XR_002958056.1:n.904-96del
NM_000023.4:c.386-96del MANE Select NP_000014.1:n.386-96del
NM_001135697.3:c.386-96del NP_001129169.1:n.386-96del
NR_135553.2:n.422-96del