Canonical Allele Identifier: CA2576072785
Gene: GAN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81365147G>T , CM000678.2:g.81365147G>T GRCh38
NC_000016.9:g.81398752G>T , CM000678.1:g.81398752G>T GRCh37
NC_000016.8:g.79956253G>T NCBI36
NG_009007.1:g.55182G>T , LRG_242:g.55182G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000648349.2:c.*1081+37G>T ENSP00000498114.1:n.*1081+37G>T
ENST00000648994.2:c.1373+37G>T MANE Select ENSP00000497351.1:n.1373+37G>T
ENST00000650388.1:c.907+37G>T ENSP00000498081.1:n.907+37G>T
ENST00000568107.2:c.1373+37G>T ENSP00000476795.1:n.1373+37G>T
NM_022041.3:c.1373+37G>T , LRG_242t1:c.1373+37G>T NP_071324.1:n.1373+37G>T
XM_017023734.1:c.734+37G>T XP_016879223.1:n.734+37G>T
NM_001377486.1:c.734+37G>T NP_001364415.1:n.734+37G>T
NM_022041.4:c.1373+37G>T MANE Select NP_071324.1:n.1373+37G>T