Canonical Allele Identifier: CA500828416
Gene: SGCA HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.48245772C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50168411C>G , CM000679.2:g.50168411C>G GRCh38
NC_000017.10:g.48245772C>G , CM000679.1:g.48245772C>G GRCh37
NC_000017.9:g.45600771C>G NCBI36
NG_008889.1:g.7407C>G , LRG_203:g.7407C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000504073.2:c.423C>G ENSP00000422030.2:p.Arg141=
ENST00000511303.6:n.148C>G
ENST00000512526.2:c.414C>G ENSP00000426606.2:n.414C>G
ENST00000682109.1:c.303C>G ENSP00000508041.1:p.Arg101=
ENST00000683226.1:n.133C>G
ENST00000683294.1:c.423C>G ENSP00000508134.1:p.Arg141=
ENST00000262018.8:c.423C>G MANE Select ENSP00000262018.3:p.Arg141=
ENST00000262018.7:c.423C>G ENSP00000262018.3:p.Arg141=
ENST00000344627.10:c.423C>G ENSP00000345522.6:p.Arg141=
ENST00000502555.5:c.*82C>G ENSP00000422817.1:n.*82C>G
ENST00000511303.5:c.144C>G ENSP00000426104.1:p.Arg48=
ENST00000512526.1:c.258C>G
ENST00000513821.5:c.423C>G ENSP00000426571.1:p.Arg141=
ENST00000513942.5:n.214C>G
ENST00000514934.1:c.*129C>G ENSP00000423168.1:n.*129C>G
NM_000023.2:c.423C>G , LRG_203t1:c.423C>G NP_000014.1:p.Arg141=
NM_001135697.1:c.423C>G NP_001129169.1:p.Arg141=
XM_011525120.1:c.423C>G XP_011523422.1:p.Arg141=
XM_011525121.1:c.423C>G XP_011523423.1:p.Arg141=
XM_011525122.1:c.423C>G XP_011523424.1:p.Arg141=
XM_011525123.1:c.423C>G XP_011523425.1:p.Arg141=
XM_011525124.1:c.117C>G XP_011523426.1:p.Arg39=
XR_934517.1:n.489C>G
NM_000023.3:c.423C>G NP_000014.1:p.Arg141=
NM_001135697.2:c.423C>G NP_001129169.1:p.Arg141=
NR_135553.1:n.479C>G
XM_011525120.2:c.585C>G XP_011523422.2:p.Arg195=
XM_011525121.2:c.585C>G XP_011523423.2:p.Arg195=
XM_011525122.2:c.585C>G XP_011523424.2:p.Arg195=
XM_011525123.2:c.585C>G XP_011523425.2:p.Arg195=
XM_011525124.2:c.117C>G XP_011523426.1:p.Arg39=
XM_024450873.1:c.117C>G XP_024306641.1:p.Arg39=
XR_002958056.1:n.941C>G
NM_000023.4:c.423C>G MANE Select NP_000014.1:p.Arg141=
NM_001135697.3:c.423C>G NP_001129169.1:p.Arg141=
NR_135553.2:n.459C>G