Canonical Allele Identifier: CA2237016649
Gene: GAN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81315433C= , CM000678.2:g.81315433C= GRCh38
NC_000016.9:g.81349038C= , CM000678.1:g.81349038C= GRCh37
NC_000016.8:g.79906539C= NCBI36
NG_009007.1:g.5468C= , LRG_242:g.5468C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000648349.2:c.167+153C= ENSP00000498114.1:n.167+153C=
ENST00000648994.2:c.167+153C= MANE Select ENSP00000497351.1:n.167+153C=
ENST00000650388.1:c.167+153C= ENSP00000498081.1:n.167+153C=
ENST00000674788.1:n.292+153C=
ENST00000568107.2:c.167+153C= ENSP00000476795.1:n.167+153C=
NM_022041.3:c.167+153C= , LRG_242t1:c.167+153C= NP_071324.1:n.167+153C=
XM_017023734.1:c.-358+153C= XP_016879223.1:n.-358+153C=
NM_001377486.1:c.-358+153C= NP_001364415.1:n.-358+153C=
NM_022041.4:c.167+153C= MANE Select NP_071324.1:n.167+153C=