Canonical Allele Identifier: CA2534693260

Gene: MN1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.27750380T>C , CM000684.2:g.27750380T>C	GRCh38
NC_000022.10:g.28146368T>C , CM000684.1:g.28146368T>C	GRCh37
NC_000022.9:g.26476368T>C	NCBI36
NG_023258.1:g.56119A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703102.1:n.1023A>G
ENST00000302326.5:c.*535A>G MANE Select	ENSP00000304956.4:n.*535A>G
ENST00000302326.4:c.*535A>G	ENSP00000304956.4:n.*535A>G
ENST00000424656.1:c.456-152A>G
NM_002430.2:c.*535A>G	NP_002421.3:n.*535A>G
NM_002430.3:c.*535A>G MANE Select	NP_002421.3:n.*535A>G