Canonical Allele Identifier: CA2841979709

Gene: SGCA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50168346G>T , CM000679.2:g.50168346G>T	GRCh38
NC_000017.10:g.48245707G>T , CM000679.1:g.48245707G>T	GRCh37
NC_000017.9:g.45600706G>T	NCBI36
NG_008889.1:g.7342G>T , LRG_203:g.7342G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504073.2:c.386-28G>T	ENSP00000422030.2:n.386-28G>T
ENST00000511303.6:n.111-28G>T
ENST00000512526.2:c.377-28G>T	ENSP00000426606.2:n.377-28G>T
ENST00000682109.1:c.266-28G>T	ENSP00000508041.1:n.266-28G>T
ENST00000683226.1:n.96-28G>T
ENST00000683294.1:c.386-28G>T	ENSP00000508134.1:n.386-28G>T
ENST00000262018.8:c.386-28G>T MANE Select	ENSP00000262018.3:n.386-28G>T
ENST00000262018.7:c.386-28G>T	ENSP00000262018.3:n.386-28G>T
ENST00000344627.10:c.386-28G>T	ENSP00000345522.6:n.386-28G>T
ENST00000502555.5:c.*45-28G>T	ENSP00000422817.1:n.*45-28G>T
ENST00000511303.5:c.107-28G>T	ENSP00000426104.1:n.107-28G>T
ENST00000512526.1:c.221-28G>T
ENST00000513821.5:c.386-28G>T	ENSP00000426571.1:n.386-28G>T
ENST00000513942.5:n.177-28G>T
ENST00000514934.1:c.*92-28G>T	ENSP00000423168.1:n.*92-28G>T
NM_000023.2:c.386-28G>T , LRG_203t1:c.386-28G>T	NP_000014.1:n.386-28G>T
NM_001135697.1:c.386-28G>T	NP_001129169.1:n.386-28G>T
XM_011525120.1:c.386-28G>T	XP_011523422.1:n.386-28G>T
XM_011525121.1:c.386-28G>T	XP_011523423.1:n.386-28G>T
XM_011525122.1:c.386-28G>T	XP_011523424.1:n.386-28G>T
XM_011525123.1:c.386-28G>T	XP_011523425.1:n.386-28G>T
XM_011525124.1:c.80-28G>T	XP_011523426.1:n.80-28G>T
XR_934517.1:n.452-28G>T
NM_000023.3:c.386-28G>T	NP_000014.1:n.386-28G>T
NM_001135697.2:c.386-28G>T	NP_001129169.1:n.386-28G>T
NR_135553.1:n.442-28G>T
XM_011525120.2:c.548-28G>T	XP_011523422.2:n.548-28G>T
XM_011525121.2:c.548-28G>T	XP_011523423.2:n.548-28G>T
XM_011525122.2:c.548-28G>T	XP_011523424.2:n.548-28G>T
XM_011525123.2:c.548-28G>T	XP_011523425.2:n.548-28G>T
XM_011525124.2:c.80-28G>T	XP_011523426.1:n.80-28G>T
XM_024450873.1:c.80-28G>T	XP_024306641.1:n.80-28G>T
XR_002958056.1:n.904-28G>T
NM_000023.4:c.386-28G>T MANE Select	NP_000014.1:n.386-28G>T
NM_001135697.3:c.386-28G>T	NP_001129169.1:n.386-28G>T
NR_135553.2:n.422-28G>T