Canonical Allele Identifier: CA496698878
Gene: GAN HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.81388069G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81354464G>C , CM000678.2:g.81354464G>C GRCh38
NC_000016.9:g.81388069G>C , CM000678.1:g.81388069G>C GRCh37
NC_000016.8:g.79945570G>C NCBI36
NG_009007.1:g.44499G>C , LRG_242:g.44499G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000648349.2:c.*50G>C ENSP00000498114.1:n.*50G>C
ENST00000648994.2:c.342G>C MANE Select ENSP00000497351.1:p.Leu114=
ENST00000650388.1:c.168-2321G>C ENSP00000498081.1:n.168-2321G>C
ENST00000674788.1:n.467G>C
ENST00000568107.2:c.342G>C ENSP00000476795.1:p.Leu114=
NM_022041.3:c.342G>C , LRG_242t1:c.342G>C NP_071324.1:p.Leu114=
XM_017023734.1:c.-298G>C XP_016879223.1:n.-298G>C
NM_001377486.1:c.-298G>C NP_001364415.1:n.-298G>C
NM_022041.4:c.342G>C MANE Select NP_071324.1:p.Leu114=