Canonical Allele Identifier: CA2638703139

Gene: SGCA

Linked Data

• gnomAD v4: 17-50167291-TTGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50167295_50167297del , CM000679.2:g.50167295_50167297del	GRCh38
NC_000017.10:g.48244656_48244658del , CM000679.1:g.48244656_48244658del	GRCh37
NC_000017.9:g.45599655_45599657del	NCBI36
NG_008889.1:g.6291_6293del , LRG_203:g.6291_6293del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504073.2:c.38-73_38-71del	ENSP00000422030.2:n.38-73_38-71del
ENST00000511303.6:n.38-652_38-650del
ENST00000512526.2:c.38-73_38-71del	ENSP00000426606.2:n.38-73_38-71del
ENST00000682109.1:c.38-287_38-285del	ENSP00000508041.1:n.38-287_38-285del
ENST00000683294.1:c.38-73_38-71del	ENSP00000508134.1:n.38-73_38-71del
ENST00000262018.8:c.38-73_38-71del MANE Select	ENSP00000262018.3:n.38-73_38-71del
ENST00000262018.7:c.38-73_38-71del	ENSP00000262018.3:n.38-73_38-71del
ENST00000344627.10:c.38-73_38-71del	ENSP00000345522.6:n.38-73_38-71del
ENST00000502555.5:c.38-73_38-71del	ENSP00000422817.1:n.38-73_38-71del
ENST00000511303.5:c.34-652_34-650del	ENSP00000426104.1:n.34-652_34-650del
ENST00000513821.5:c.38-73_38-71del	ENSP00000426571.1:n.38-73_38-71del
ENST00000513942.5:n.104-652_104-650del
ENST00000514934.1:c.97-73_97-71del	ENSP00000423168.1:n.97-73_97-71del
NM_000023.2:c.38-73_38-71del , LRG_203t1:c.38-73_38-71del	NP_000014.1:n.38-73_38-71del
NM_001135697.1:c.38-73_38-71del	NP_001129169.1:n.38-73_38-71del
XM_011525120.1:c.38-73_38-71del	XP_011523422.1:n.38-73_38-71del
XM_011525121.1:c.38-73_38-71del	XP_011523423.1:n.38-73_38-71del
XM_011525122.1:c.38-73_38-71del	XP_011523424.1:n.38-73_38-71del
XM_011525123.1:c.38-73_38-71del	XP_011523425.1:n.38-73_38-71del
XM_011525124.1:c.-114-73_-114-71del	XP_011523426.1:n.-114-73_-114-71del
XR_934517.1:n.104-73_104-71del
NM_000023.3:c.38-73_38-71del	NP_000014.1:n.38-73_38-71del
NM_001135697.2:c.38-73_38-71del	NP_001129169.1:n.38-73_38-71del
NR_135553.1:n.94-73_94-71del
XM_011525120.2:c.200-73_200-71del	XP_011523422.2:n.200-73_200-71del
XM_011525121.2:c.200-73_200-71del	XP_011523423.2:n.200-73_200-71del
XM_011525122.2:c.200-73_200-71del	XP_011523424.2:n.200-73_200-71del
XM_011525123.2:c.200-73_200-71del	XP_011523425.2:n.200-73_200-71del
XM_011525124.2:c.-114-73_-114-71del	XP_011523426.1:n.-114-73_-114-71del
XM_024450873.1:c.-114-73_-114-71del	XP_024306641.1:n.-114-73_-114-71del
XR_002958056.1:n.556-73_556-71del
NM_000023.4:c.38-73_38-71del MANE Select	NP_000014.1:n.38-73_38-71del
NM_001135697.3:c.38-73_38-71del	NP_001129169.1:n.38-73_38-71del
NR_135553.2:n.74-73_74-71del