Canonical Allele Identifier: CA396891416

Gene: GAN

Linked Data

• dbSNP Id: rs1597407355
• gnomAD v4: 16-81365430-G-C
• MyVariant Identifiers: chr16:g.81399035G>C (hg19) ; chr16:g.81365430G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81365430G>C , CM000678.2:g.81365430G>C	GRCh38
NC_000016.9:g.81399035G>C , CM000678.1:g.81399035G>C	GRCh37
NC_000016.8:g.79956536G>C	NCBI36
NG_009007.1:g.55465G>C , LRG_242:g.55465G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000648349.2:c.*1162G>C	ENSP00000498114.1:n.*1162G>C
ENST00000648994.2:c.1454G>C MANE Select	ENSP00000497351.1:p.Ser485Thr
ENST00000650388.1:c.988G>C	ENSP00000498081.1:n.988G>C
ENST00000567335.1:n.12G>C
ENST00000568107.2:c.1454G>C	ENSP00000476795.1:p.Ser485Thr
NM_022041.3:c.1454G>C , LRG_242t1:c.1454G>C	NP_071324.1:p.Ser485Thr
XM_017023734.1:c.815G>C	XP_016879223.1:p.Ser272Thr
NM_001377486.1:c.815G>C	NP_001364415.1:p.Ser272Thr
NM_022041.4:c.1454G>C MANE Select	NP_071324.1:p.Ser485Thr