Canonical Allele Identifier: CA2638707553

Gene: SGCA

Linked Data

• gnomAD v4: 17-50170064-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50170066del , CM000679.2:g.50170066del	GRCh38
NC_000017.10:g.48247427del , CM000679.1:g.48247427del	GRCh37
NC_000017.9:g.45602426del	NCBI36
NG_008889.1:g.9062del , LRG_203:g.9062del

Transcript Alleles

HGVS	Amino-acid change
ENST00000504073.2:c.598-77del	ENSP00000422030.2:n.598-77del
ENST00000511303.6:n.310-574del
ENST00000512526.2:c.576-574del	ENSP00000426606.2:n.576-574del
ENST00000682109.1:c.628-77del	ENSP00000508041.1:n.628-77del
ENST00000683226.1:n.1269del
ENST00000683294.1:c.750del	ENSP00000508134.1:p.Trp251GlyfsTer?
ENST00000683544.1:n.37del
ENST00000262018.8:c.748-77del MANE Select	ENSP00000262018.3:n.748-77del
ENST00000262018.7:c.748-77del	ENSP00000262018.3:n.748-77del
ENST00000344627.10:c.585-574del	ENSP00000345522.6:n.585-574del
ENST00000504073.1:c.65-77del
ENST00000511303.5:c.306-574del	ENSP00000426104.1:n.306-574del
ENST00000512526.1:c.420-574del
ENST00000513821.5:c.748-574del	ENSP00000426571.1:n.748-574del
ENST00000513942.5:n.376-574del
NM_000023.2:c.748-77del , LRG_203t1:c.748-77del	NP_000014.1:n.748-77del
NM_001135697.1:c.585-574del	NP_001129169.1:n.585-574del
XM_011525120.1:c.748-77del	XP_011523422.1:n.748-77del
XM_011525121.1:c.598-77del	XP_011523423.1:n.598-77del
XM_011525122.1:c.748-574del	XP_011523424.1:n.748-574del
XM_011525123.1:c.585-574del	XP_011523425.1:n.585-574del
XM_011525124.1:c.442-77del	XP_011523426.1:n.442-77del
XR_934517.1:n.814-574del
NM_000023.3:c.748-77del	NP_000014.1:n.748-77del
NM_001135697.2:c.585-574del	NP_001129169.1:n.585-574del
NR_135553.1:n.804-574del
XM_011525120.2:c.910-77del	XP_011523422.2:n.910-77del
XM_011525121.2:c.760-77del	XP_011523423.2:n.760-77del
XM_011525122.2:c.910-574del	XP_011523424.2:n.910-574del
XM_011525123.2:c.747-574del	XP_011523425.2:n.747-574del
XM_011525124.2:c.442-77del	XP_011523426.1:n.442-77del
XM_024450873.1:c.442-77del	XP_024306641.1:n.442-77del
XR_002958056.1:n.1268del
NM_000023.4:c.748-77del MANE Select	NP_000014.1:n.748-77del
NM_001135697.3:c.585-574del	NP_001129169.1:n.585-574del
NR_135553.2:n.784-574del