Canonical Allele Identifier: CA2638704467

Gene: SGCA

Linked Data

• gnomAD v4: 17-50168296-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50168296G>T , CM000679.2:g.50168296G>T	GRCh38
NC_000017.10:g.48245657G>T , CM000679.1:g.48245657G>T	GRCh37
NC_000017.9:g.45600656G>T	NCBI36
NG_008889.1:g.7292G>T , LRG_203:g.7292G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000504073.2:c.386-78G>T	ENSP00000422030.2:n.386-78G>T
ENST00000511303.6:n.111-78G>T
ENST00000512526.2:c.377-78G>T	ENSP00000426606.2:n.377-78G>T
ENST00000682109.1:c.266-78G>T	ENSP00000508041.1:n.266-78G>T
ENST00000683226.1:n.96-78G>T
ENST00000683294.1:c.386-78G>T	ENSP00000508134.1:n.386-78G>T
ENST00000262018.8:c.386-78G>T MANE Select	ENSP00000262018.3:n.386-78G>T
ENST00000262018.7:c.386-78G>T	ENSP00000262018.3:n.386-78G>T
ENST00000344627.10:c.386-78G>T	ENSP00000345522.6:n.386-78G>T
ENST00000502555.5:c.*45-78G>T	ENSP00000422817.1:n.*45-78G>T
ENST00000511303.5:c.107-78G>T	ENSP00000426104.1:n.107-78G>T
ENST00000512526.1:c.221-78G>T
ENST00000513821.5:c.386-78G>T	ENSP00000426571.1:n.386-78G>T
ENST00000513942.5:n.177-78G>T
ENST00000514934.1:c.*92-78G>T	ENSP00000423168.1:n.*92-78G>T
NM_000023.2:c.386-78G>T , LRG_203t1:c.386-78G>T	NP_000014.1:n.386-78G>T
NM_001135697.1:c.386-78G>T	NP_001129169.1:n.386-78G>T
XM_011525120.1:c.386-78G>T	XP_011523422.1:n.386-78G>T
XM_011525121.1:c.386-78G>T	XP_011523423.1:n.386-78G>T
XM_011525122.1:c.386-78G>T	XP_011523424.1:n.386-78G>T
XM_011525123.1:c.386-78G>T	XP_011523425.1:n.386-78G>T
XM_011525124.1:c.80-78G>T	XP_011523426.1:n.80-78G>T
XR_934517.1:n.452-78G>T
NM_000023.3:c.386-78G>T	NP_000014.1:n.386-78G>T
NM_001135697.2:c.386-78G>T	NP_001129169.1:n.386-78G>T
NR_135553.1:n.442-78G>T
XM_011525120.2:c.548-78G>T	XP_011523422.2:n.548-78G>T
XM_011525121.2:c.548-78G>T	XP_011523423.2:n.548-78G>T
XM_011525122.2:c.548-78G>T	XP_011523424.2:n.548-78G>T
XM_011525123.2:c.548-78G>T	XP_011523425.2:n.548-78G>T
XM_011525124.2:c.80-78G>T	XP_011523426.1:n.80-78G>T
XM_024450873.1:c.80-78G>T	XP_024306641.1:n.80-78G>T
XR_002958056.1:n.904-78G>T
NM_000023.4:c.386-78G>T MANE Select	NP_000014.1:n.386-78G>T
NM_001135697.3:c.386-78G>T	NP_001129169.1:n.386-78G>T
NR_135553.2:n.422-78G>T