Canonical Allele Identifier: CA2237033593
Gene: GAN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81354774A= , CM000678.2:g.81354774A= GRCh38
NC_000016.9:g.81388379A= , CM000678.1:g.81388379A= GRCh37
NC_000016.8:g.79945880A= NCBI36
NG_009007.1:g.44809A= , LRG_242:g.44809A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000648349.2:c.*341+19A= ENSP00000498114.1:n.*341+19A=
ENST00000648994.2:c.633+19A= MANE Select ENSP00000497351.1:n.633+19A=
ENST00000650388.1:c.168-2011A= ENSP00000498081.1:n.168-2011A=
ENST00000674788.1:n.777A=
ENST00000568107.2:c.633+19A= ENSP00000476795.1:n.633+19A=
NM_022041.3:c.633+19A= , LRG_242t1:c.633+19A= NP_071324.1:n.633+19A=
XM_017023734.1:c.-7+19A= XP_016879223.1:n.-7+19A=
NM_001377486.1:c.-7+19A= NP_001364415.1:n.-7+19A=
NM_022041.4:c.633+19A= MANE Select NP_071324.1:n.633+19A=