Canonical Allele Identifier: CA2576072608
Gene: GAN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81354372T>C , CM000678.2:g.81354372T>C GRCh38
NC_000016.9:g.81387977T>C , CM000678.1:g.81387977T>C GRCh37
NC_000016.8:g.79945478T>C NCBI36
NG_009007.1:g.44407T>C , LRG_242:g.44407T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000648349.2:c.168-33T>C ENSP00000498114.1:n.168-33T>C
ENST00000648994.2:c.283-33T>C MANE Select ENSP00000497351.1:n.283-33T>C
ENST00000650388.1:c.168-2413T>C ENSP00000498081.1:n.168-2413T>C
ENST00000674788.1:n.408-33T>C
ENST00000568107.2:c.283-33T>C ENSP00000476795.1:n.283-33T>C
NM_022041.3:c.283-33T>C , LRG_242t1:c.283-33T>C NP_071324.1:n.283-33T>C
XM_017023734.1:c.-357-33T>C XP_016879223.1:n.-357-33T>C
NM_001377486.1:c.-357-33T>C NP_001364415.1:n.-357-33T>C
NM_022041.4:c.283-33T>C MANE Select NP_071324.1:n.283-33T>C