Canonical Allele Identifier: CA411033141

Gene: MN1

Linked Data

• MyVariant Identifiers: chr22:g.28146965A>T (hg19) ; chr22:g.27750977A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.27750977A>T , CM000684.2:g.27750977A>T	GRCh38
NC_000022.10:g.28146965A>T , CM000684.1:g.28146965A>T	GRCh37
NC_000022.9:g.26476965A>T	NCBI36
NG_023258.1:g.55522T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703102.1:n.426T>A
ENST00000302326.5:c.3901T>A MANE Select	ENSP00000304956.4:p.Trp1301Arg
ENST00000302326.4:c.3901T>A	ENSP00000304956.4:p.Trp1301Arg
ENST00000424656.1:c.254T>A
ENST00000497225.1:n.257T>A
NM_002430.2:c.3901T>A	NP_002421.3:p.Trp1301Arg
NM_002430.3:c.3901T>A MANE Select	NP_002421.3:p.Trp1301Arg