Canonical Allele Identifier: CA2237043268
Gene: GAN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81358200A= , CM000678.2:g.81358200A= GRCh38
NC_000016.9:g.81391805A= , CM000678.1:g.81391805A= GRCh37
NC_000016.8:g.79949306A= NCBI36
NG_009007.1:g.48235A= , LRG_242:g.48235A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000648349.2:c.*681+269A= ENSP00000498114.1:n.*681+269A=
ENST00000648994.2:c.973+269A= MANE Select ENSP00000497351.1:n.973+269A=
ENST00000650388.1:c.507+269A= ENSP00000498081.1:n.507+269A=
ENST00000568107.2:c.973+269A= ENSP00000476795.1:n.973+269A=
NM_022041.3:c.973+269A= , LRG_242t1:c.973+269A= NP_071324.1:n.973+269A=
XM_017023734.1:c.334+269A= XP_016879223.1:n.334+269A=
NM_001377486.1:c.334+269A= NP_001364415.1:n.334+269A=
NM_022041.4:c.973+269A= MANE Select NP_071324.1:n.973+269A=