Canonical Allele Identifier: CA2525566668

Gene: MN1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.27750786_27750794del , CM000684.2:g.27750786_27750794del	GRCh38
NC_000022.10:g.28146774_28146782del , CM000684.1:g.28146774_28146782del	GRCh37
NC_000022.9:g.26476774_26476782del	NCBI36
NG_023258.1:g.55705_55713del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703102.1:n.609_617del
ENST00000302326.5:c.*121_*129del MANE Select	ENSP00000304956.4:n.*121_*129del
ENST00000302326.4:c.*121_*129del	ENSP00000304956.4:n.*121_*129del
ENST00000424656.1:c.437_445del
ENST00000497225.1:n.440_448del
NM_002430.2:c.*121_*129del	NP_002421.3:n.*121_*129del
NM_002430.3:c.*121_*129del MANE Select	NP_002421.3:n.*121_*129del