Canonical Allele Identifier: CA2263905312

Gene: SGCA

Linked Data

• dbSNP Id: rs1905054562

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50167891_50167892insT , CM000679.2:g.50167891_50167892insT	GRCh38
NC_000017.10:g.48245252_48245253insT , CM000679.1:g.48245252_48245253insT	GRCh37
NC_000017.9:g.45600251_45600252insT	NCBI36
NG_008889.1:g.6887_6888insT , LRG_203:g.6887_6888insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504073.2:c.313-56_313-55insT	ENSP00000422030.2:n.313-56_313-55insT
ENST00000511303.6:n.38-56_38-55insT
ENST00000512526.2:c.304-56_304-55insT	ENSP00000426606.2:n.304-56_304-55insT
ENST00000682109.1:c.193-56_193-55insT	ENSP00000508041.1:n.193-56_193-55insT
ENST00000683226.1:n.23-56_23-55insT
ENST00000683294.1:c.313-56_313-55insT	ENSP00000508134.1:n.313-56_313-55insT
ENST00000262018.8:c.313-56_313-55insT MANE Select	ENSP00000262018.3:n.313-56_313-55insT
ENST00000262018.7:c.313-56_313-55insT	ENSP00000262018.3:n.313-56_313-55insT
ENST00000344627.10:c.313-56_313-55insT	ENSP00000345522.6:n.313-56_313-55insT
ENST00000502555.5:c.158-56_158-55insT	ENSP00000422817.1:n.158-56_158-55insT
ENST00000511303.5:c.34-56_34-55insT	ENSP00000426104.1:n.34-56_34-55insT
ENST00000512526.1:c.148-56_148-55insT
ENST00000513821.5:c.313-56_313-55insT	ENSP00000426571.1:n.313-56_313-55insT
ENST00000513942.5:n.104-56_104-55insT
ENST00000514934.1:c.*19-56_*19-55insT	ENSP00000423168.1:n.*19-56_*19-55insT
NM_000023.2:c.313-56_313-55insT , LRG_203t1:c.313-56_313-55insT	NP_000014.1:n.313-56_313-55insT
NM_001135697.1:c.313-56_313-55insT	NP_001129169.1:n.313-56_313-55insT
XM_011525120.1:c.313-56_313-55insT	XP_011523422.1:n.313-56_313-55insT
XM_011525121.1:c.313-56_313-55insT	XP_011523423.1:n.313-56_313-55insT
XM_011525122.1:c.313-56_313-55insT	XP_011523424.1:n.313-56_313-55insT
XM_011525123.1:c.313-56_313-55insT	XP_011523425.1:n.313-56_313-55insT
XM_011525124.1:c.7-56_7-55insT	XP_011523426.1:n.7-56_7-55insT
XR_934517.1:n.379-56_379-55insT
NM_000023.3:c.313-56_313-55insT	NP_000014.1:n.313-56_313-55insT
NM_001135697.2:c.313-56_313-55insT	NP_001129169.1:n.313-56_313-55insT
NR_135553.1:n.369-56_369-55insT
XM_011525120.2:c.475-56_475-55insT	XP_011523422.2:n.475-56_475-55insT
XM_011525121.2:c.475-56_475-55insT	XP_011523423.2:n.475-56_475-55insT
XM_011525122.2:c.475-56_475-55insT	XP_011523424.2:n.475-56_475-55insT
XM_011525123.2:c.475-56_475-55insT	XP_011523425.2:n.475-56_475-55insT
XM_011525124.2:c.7-56_7-55insT	XP_011523426.1:n.7-56_7-55insT
XM_024450873.1:c.7-56_7-55insT	XP_024306641.1:n.7-56_7-55insT
XR_002958056.1:n.831-56_831-55insT
NM_000023.4:c.313-56_313-55insT MANE Select	NP_000014.1:n.313-56_313-55insT
NM_001135697.3:c.313-56_313-55insT	NP_001129169.1:n.313-56_313-55insT
NR_135553.2:n.349-56_349-55insT