Canonical Allele Identifier: CA2263906375
Gene: SGCA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50169871C= , CM000679.2:g.50169871C= GRCh38
NC_000017.10:g.48247232C= , CM000679.1:g.48247232C= GRCh37
NC_000017.9:g.45602231C= NCBI36
NG_008889.1:g.8867C= , LRG_203:g.8867C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000504073.2:c.598-272C= ENSP00000422030.2:n.598-272C=
ENST00000511303.6:n.310-769C=
ENST00000512526.2:c.576-769C= ENSP00000426606.2:n.576-769C=
ENST00000682109.1:c.628-272C= ENSP00000508041.1:n.628-272C=
ENST00000683226.1:n.1074C=
ENST00000683294.1:c.748-193C= ENSP00000508134.1:n.748-193C=
ENST00000262018.8:c.748-272C= MANE Select ENSP00000262018.3:n.748-272C=
ENST00000262018.7:c.748-272C= ENSP00000262018.3:n.748-272C=
ENST00000344627.10:c.585-769C= ENSP00000345522.6:n.585-769C=
ENST00000502555.5:c.*1023C= ENSP00000422817.1:n.*1023C=
ENST00000504073.1:c.65-272C=
ENST00000511303.5:c.306-769C= ENSP00000426104.1:n.306-769C=
ENST00000512526.1:c.420-769C=
ENST00000513821.5:c.747+617C= ENSP00000426571.1:n.747+617C=
ENST00000513942.5:n.376-769C=
NM_000023.2:c.748-272C= , LRG_203t1:c.748-272C= NP_000014.1:n.748-272C=
NM_001135697.1:c.585-769C= NP_001129169.1:n.585-769C=
XM_011525120.1:c.748-272C= XP_011523422.1:n.748-272C=
XM_011525121.1:c.598-272C= XP_011523423.1:n.598-272C=
XM_011525122.1:c.747+617C= XP_011523424.1:n.747+617C=
XM_011525123.1:c.585-769C= XP_011523425.1:n.585-769C=
XM_011525124.1:c.442-272C= XP_011523426.1:n.442-272C=
XR_934517.1:n.813+617C=
NM_000023.3:c.748-272C= NP_000014.1:n.748-272C=
NM_001135697.2:c.585-769C= NP_001129169.1:n.585-769C=
NR_135553.1:n.803+617C=
XM_011525120.2:c.910-272C= XP_011523422.2:n.910-272C=
XM_011525121.2:c.760-272C= XP_011523423.2:n.760-272C=
XM_011525122.2:c.909+617C= XP_011523424.2:n.909+617C=
XM_011525123.2:c.747-769C= XP_011523425.2:n.747-769C=
XM_011525124.2:c.442-272C= XP_011523426.1:n.442-272C=
XM_024450873.1:c.442-272C= XP_024306641.1:n.442-272C=
XR_002958056.1:n.1266-193C=
NM_000023.4:c.748-272C= MANE Select NP_000014.1:n.748-272C=
NM_001135697.3:c.585-769C= NP_001129169.1:n.585-769C=
NR_135553.2:n.783+617C=