Canonical Allele Identifier: CA2237031742

Gene: GAN

Linked Data

• dbSNP Id: rs1910408491

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81354258G>C , CM000678.2:g.81354258G>C	GRCh38
NC_000016.9:g.81387863G>C , CM000678.1:g.81387863G>C	GRCh37
NC_000016.8:g.79945364G>C	NCBI36
NG_009007.1:g.44293G>C , LRG_242:g.44293G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648349.2:c.168-147G>C	ENSP00000498114.1:n.168-147G>C
ENST00000648994.2:c.283-147G>C MANE Select	ENSP00000497351.1:n.283-147G>C
ENST00000650388.1:c.168-2527G>C	ENSP00000498081.1:n.168-2527G>C
ENST00000674788.1:n.408-147G>C
ENST00000568107.2:c.283-147G>C	ENSP00000476795.1:n.283-147G>C
NM_022041.3:c.283-147G>C , LRG_242t1:c.283-147G>C	NP_071324.1:n.283-147G>C
XM_017023734.1:c.-357-147G>C	XP_016879223.1:n.-357-147G>C
NM_001377486.1:c.-357-147G>C	NP_001364415.1:n.-357-147G>C
NM_022041.4:c.283-147G>C MANE Select	NP_071324.1:n.283-147G>C