Canonical Allele Identifier: CA2818640034

Gene: MN1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.27750754_27750755insGGTGTGGAAACTCT , CM000684.2:g.27750754_27750755insGGTGTGGAAACTCT	GRCh38
NC_000022.10:g.28146742_28146743insGGTGTGGAAACTCT , CM000684.1:g.28146742_28146743insGGTGTGGAAACTCT	GRCh37
NC_000022.9:g.26476742_26476743insGGTGTGGAAACTCT	NCBI36
NG_023258.1:g.55744_55745insAGAGTTTCCACACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703102.1:n.648_649insAGAGTTTCCACACC
ENST00000302326.5:c.*160_*161insAGAGTTTCCACACC MANE Select	ENSP00000304956.4:n.*160_*161insAGAGTTTCCACACC
ENST00000302326.4:c.*160_*161insAGAGTTTCCACACC	ENSP00000304956.4:n.*160_*161insAGAGTTTCCACACC
ENST00000424656.1:c.455+21_455+22insAGAGTTTCCACACC
ENST00000497225.1:n.479_480insAGAGTTTCCACACC
NM_002430.2:c.*160_*161insAGAGTTTCCACACC	NP_002421.3:n.*160_*161insAGAGTTTCCACACC
NM_002430.3:c.*160_*161insAGAGTTTCCACACC MANE Select	NP_002421.3:n.*160_*161insAGAGTTTCCACACC