Canonical Allele Identifier: CA2818639998

Gene: MN1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.27750444del , CM000684.2:g.27750444del	GRCh38
NC_000022.10:g.28146432del , CM000684.1:g.28146432del	GRCh37
NC_000022.9:g.26476432del	NCBI36
NG_023258.1:g.56057del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703102.1:n.961del
ENST00000302326.5:c.*473del MANE Select	ENSP00000304956.4:n.*473del
ENST00000302326.4:c.*473del	ENSP00000304956.4:n.*473del
ENST00000424656.1:c.456-214del
NM_002430.2:c.*473del	NP_002421.3:n.*473del
NM_002430.3:c.*473del MANE Select	NP_002421.3:n.*473del