Canonical Allele Identifier: CA2399817851

Gene: MN1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.27750446_27750447delinsCA , CM000684.2:g.27750446_27750447delinsCA	GRCh38
NC_000022.10:g.28146434_28146435delinsCA , CM000684.1:g.28146434_28146435delinsCA	GRCh37
NC_000022.9:g.26476434_26476435delinsCA	NCBI36
NG_023258.1:g.56052_56053delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703102.1:n.956_957delinsTG
ENST00000302326.5:c.*468_*469delinsTG MANE Select	ENSP00000304956.4:n.*468_*469delinsTG
ENST00000302326.4:c.*468_*469delinsTG	ENSP00000304956.4:n.*468_*469delinsTG
ENST00000424656.1:c.456-219_456-218delinsTG
NM_002430.2:c.*468_*469delinsTG	NP_002421.3:n.*468_*469delinsTG
NM_002430.3:c.*468_*469delinsTG MANE Select	NP_002421.3:n.*468_*469delinsTG