Canonical Allele Identifier: CA1685978702
Gene: C1GALT1 HGNC NCBI

Linked Data

dbSNP Id: rs910773734

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.7233806T>A , CM000669.2:g.7233806T>A GRCh38
NC_000007.13:g.7273437T>A , CM000669.1:g.7273437T>A GRCh37
NC_000007.12:g.7239962T>A NCBI36
NG_027732.1:g.56192T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000436587.7:c.-17-497T>A MANE Select ENSP00000389176.2:n.-17-497T>A
ENST00000419721.5:c.-17-497T>A ENSP00000415400.1:n.-17-497T>A
ENST00000429911.5:c.-17-497T>A ENSP00000407666.1:n.-17-497T>A
ENST00000436587.6:c.-17-497T>A ENSP00000389176.2:n.-17-497T>A
ENST00000476068.1:n.192-497T>A
NM_020156.4:c.-17-497T>A NP_064541.1:n.-17-497T>A
XM_005249812.1:c.8-497T>A XP_005249869.1:n.8-497T>A
XM_011515453.1:c.-17-497T>A XP_011513755.1:n.-17-497T>A
XM_011515454.1:c.-17-497T>A XP_011513756.1:n.-17-497T>A
XM_011515455.1:c.-17-497T>A XP_011513757.1:n.-17-497T>A
XM_011515456.1:c.-17-497T>A XP_011513758.1:n.-17-497T>A
XM_011515453.2:c.-17-497T>A XP_011513755.1:n.-17-497T>A
XM_011515455.2:c.-17-497T>A XP_011513757.1:n.-17-497T>A
XM_011515456.2:c.-17-497T>A XP_011513758.1:n.-17-497T>A
XM_017012442.1:c.-17-497T>A XP_016867931.1:n.-17-497T>A
XM_017012444.1:c.-17-497T>A XP_016867933.1:n.-17-497T>A
XM_017012445.1:c.-17-497T>A XP_016867934.1:n.-17-497T>A
XM_017012446.1:c.-17-497T>A XP_016867935.1:n.-17-497T>A
XM_017012447.1:c.-17-497T>A XP_016867936.1:n.-17-497T>A
XM_017012448.1:c.-17-497T>A XP_016867937.1:n.-17-497T>A
XM_024446838.1:c.-17-497T>A XP_024302606.1:n.-17-497T>A
NM_020156.5:c.-17-497T>A MANE Select NP_064541.1:n.-17-497T>A