Canonical Allele Identifier: CA2237033801
Gene: GAN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81354823T= , CM000678.2:g.81354823T= GRCh38
NC_000016.9:g.81388428T= , CM000678.1:g.81388428T= GRCh37
NC_000016.8:g.79945929T= NCBI36
NG_009007.1:g.44858T= , LRG_242:g.44858T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000648349.2:c.*341+68T= ENSP00000498114.1:n.*341+68T=
ENST00000648994.2:c.633+68T= MANE Select ENSP00000497351.1:n.633+68T=
ENST00000650388.1:c.168-1962T= ENSP00000498081.1:n.168-1962T=
ENST00000674788.1:n.826T=
ENST00000568107.2:c.633+68T= ENSP00000476795.1:n.633+68T=
NM_022041.3:c.633+68T= , LRG_242t1:c.633+68T= NP_071324.1:n.633+68T=
XM_017023734.1:c.-7+68T= XP_016879223.1:n.-7+68T=
NM_001377486.1:c.-7+68T= NP_001364415.1:n.-7+68T=
NM_022041.4:c.633+68T= MANE Select NP_071324.1:n.633+68T=