Canonical Allele Identifier: CA5586580

Gene: SNCG MMRN2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.86960057G>A , CM000672.2:g.86960057G>A	GRCh38
NC_000010.10:g.88719814G>A , CM000672.1:g.88719814G>A	GRCh37
NC_000010.9:g.88709794G>A	NCBI36
NG_008783.1:g.6527G>A
NG_032913.2:g.14425C>T
NG_032913.3:g.14425C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372017.4:c.220G>A (SNCG) MANE Select	ENSP00000361087.3:p.Val74Ile
ENST00000348795.8:c.272G>A (SNCG)	ENSP00000344658.4:p.Arg91His
ENST00000372017.3:c.220G>A (SNCG)	ENSP00000361087.3:p.Val74Ile
ENST00000465679.5:n.300G>A (SNCG)
ENST00000474994.2:c.-20+8985C>T (MMRN2)	ENSP00000473405.1:n.-20+8985C>T
ENST00000483064.1:n.357G>A (SNCG)
ENST00000609457.5:c.-8+8985C>T (MMRN2)	ENSP00000476378.1:n.-8+8985C>T
NM_003087.2:c.220G>A (SNCG)	NP_003078.2:p.Val74Ile
XM_006717970.2:c.-20+8985C>T (MMRN2)	XP_006718033.1:n.-20+8985C>T
XM_011540105.1:c.272G>A (SNCG)	XP_011538407.1:p.Arg91His
NM_001330120.1:c.272G>A (SNCG)	NP_001317049.1:p.Arg91His
XM_006717970.4:c.-20+8985C>T (MMRN2)	XP_006718033.1:n.-20+8985C>T
XM_024448137.1:c.242G>A (SNCG)	XP_024303905.1:p.Arg81His
NM_003087.3:c.220G>A (SNCG) MANE Select	NP_003078.2:p.Val74Ile
NM_001330120.2:c.272G>A (SNCG)	NP_001317049.1:p.Arg91His