Canonical Allele Identifier: CA2237038162
Gene: GAN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81314975A= , CM000678.2:g.81314975A= GRCh38
NC_000016.9:g.81348580A= , CM000678.1:g.81348580A= GRCh37
NC_000016.8:g.79906081A= NCBI36
NG_009007.1:g.5010A= , LRG_242:g.5010A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000648349.2:c.-139A= ENSP00000498114.1:n.-139A=
ENST00000648994.2:c.-139A= MANE Select ENSP00000497351.1:n.-139A=
ENST00000568107.2:c.-139A= ENSP00000476795.1:n.-139A=
NM_022041.3:c.-139A= , LRG_242t1:c.-139A= NP_071324.1:n.-139A=
XM_017023734.1:c.-663A= XP_016879223.1:n.-663A=
NM_001377486.1:c.-663A= NP_001364415.1:n.-663A=
NM_022041.4:c.-139A= MANE Select NP_071324.1:n.-139A=