Canonical Allele Identifier: CA147980987
Gene: MOXD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.132321978C>T , CM000668.2:g.132321978C>T GRCh38
NC_000006.11:g.132643117C>T , CM000668.1:g.132643117C>T GRCh37
NC_000006.10:g.132684810C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000367963.8:c.1305+701G>A MANE Select ENSP00000356940.3:n.1305+701G>A
ENST00000336749.3:c.1101+701G>A ENSP00000336998.3:n.1101+701G>A
ENST00000367963.7:c.1305+701G>A ENSP00000356940.3:n.1305+701G>A
ENST00000489128.1:n.427+701G>A
NM_015529.3:c.1305+701G>A NP_056344.2:n.1305+701G>A
XM_017010714.2:c.1200+701G>A XP_016866203.1:n.1200+701G>A
NM_015529.4:c.1305+701G>A MANE Select NP_056344.2:n.1305+701G>A