Canonical Allele Identifier: CA405305940

Gene: MAG

Linked Data

• MyVariant Identifiers: chr19:g.35786866A>C (hg19) ; chr19:g.35295963A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35295963A>C , CM000681.2:g.35295963A>C	GRCh38
NC_000019.9:g.35786866A>C , CM000681.1:g.35786866A>C	GRCh37
NC_000019.8:g.40478706A>C	NCBI36
NG_034078.1:g.8878A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392213.8:c.397A>C MANE Select	ENSP00000376048.2:p.Ser133Arg
ENST00000361922.8:c.397A>C	ENSP00000355234.4:p.Ser133Arg
ENST00000392213.7:c.397A>C	ENSP00000376048.2:p.Ser133Arg
ENST00000537831.2:c.322A>C	ENSP00000440695.1:p.Ser108Arg
ENST00000595791.5:c.397A>C	ENSP00000473125.1:p.Ser133Arg
ENST00000597035.5:c.176+221A>C	ENSP00000473245.1:n.176+221A>C
ENST00000600291.5:c.322A>C	ENSP00000470772.1:p.Ser108Arg
NM_001199216.1:c.322A>C	NP_001186145.1:p.Ser108Arg
NM_002361.3:c.397A>C	NP_002352.1:p.Ser133Arg
NM_080600.2:c.397A>C	NP_542167.1:p.Ser133Arg
NM_002361.4:c.397A>C MANE Select	NP_002352.1:p.Ser133Arg
NM_001199216.2:c.322A>C	NP_001186145.1:p.Ser108Arg
NM_080600.3:c.397A>C	NP_542167.1:p.Ser133Arg