Canonical Allele Identifier: CA2361261602
Gene: MAP1LC3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.34558028C= , CM000682.2:g.34558028C= GRCh38
NC_000020.10:g.33145832C= , CM000682.1:g.33145832C= GRCh37
NC_000020.9:g.32609493C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_181509.2:c.53-1180C= NP_852610.1:n.53-1180C=
NM_181509.3:c.53-1180C= NP_852610.1:n.53-1180C=
ENST00000374837.7:c.53-1180C= ENSP00000363970.3:n.53-1180C=
XM_011529083.1:c.176-710C= XP_011527385.1:n.176-710C=
XM_011529083.2:c.176-710C= XP_011527385.1:n.176-710C=
XM_011529084.1:c.176-710C= XP_011527386.1:n.176-710C=
XM_011529084.2:c.176-710C= XP_011527386.1:n.176-710C=
XM_011529085.1:c.53-710C= XP_011527387.1:n.53-710C=
XM_011529085.2:c.53-710C= XP_011527387.1:n.53-710C=