Canonical Allele Identifier: CA513939251
Gene: MN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.28146954C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750966C>A , CM000684.2:g.27750966C>A GRCh38
NC_000022.10:g.28146954C>A , CM000684.1:g.28146954C>A GRCh37
NC_000022.9:g.26476954C>A NCBI36
NG_023258.1:g.55533G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.437G>T
ENST00000302326.5:c.3912G>T MANE Select ENSP00000304956.4:p.Leu1304=
ENST00000302326.4:c.3912G>T ENSP00000304956.4:p.Leu1304=
ENST00000424656.1:c.265G>T
ENST00000497225.1:n.268G>T
NM_002430.2:c.3912G>T NP_002421.3:p.Leu1304=
NM_002430.3:c.3912G>T MANE Select NP_002421.3:p.Leu1304=