Canonical Allele Identifier: CA1685972773

Gene: C1GALT1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.7228717_7228718delinsGC , CM000669.2:g.7228717_7228718delinsGC	GRCh38
NC_000007.13:g.7268348_7268349delinsGC , CM000669.1:g.7268348_7268349delinsGC	GRCh37
NC_000007.12:g.7234873_7234874delinsGC	NCBI36
NG_027732.1:g.51103_51104delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436587.7:c.-17-5586_-17-5585delinsGC MANE Select	ENSP00000389176.2:n.-17-5586_-17-5585delinsGC
ENST00000419721.5:c.-17-5586_-17-5585delinsGC	ENSP00000415400.1:n.-17-5586_-17-5585delinsGC
ENST00000429911.5:c.-17-5586_-17-5585delinsGC	ENSP00000407666.1:n.-17-5586_-17-5585delinsGC
ENST00000436587.6:c.-17-5586_-17-5585delinsGC	ENSP00000389176.2:n.-17-5586_-17-5585delinsGC
ENST00000476068.1:n.192-5586_192-5585delinsGC
NM_020156.4:c.-17-5586_-17-5585delinsGC	NP_064541.1:n.-17-5586_-17-5585delinsGC
XM_005249812.1:c.8-5586_8-5585delinsGC	XP_005249869.1:n.8-5586_8-5585delinsGC
XM_011515453.1:c.-17-5586_-17-5585delinsGC	XP_011513755.1:n.-17-5586_-17-5585delinsGC
XM_011515454.1:c.-17-5586_-17-5585delinsGC	XP_011513756.1:n.-17-5586_-17-5585delinsGC
XM_011515455.1:c.-17-5586_-17-5585delinsGC	XP_011513757.1:n.-17-5586_-17-5585delinsGC
XM_011515456.1:c.-17-5586_-17-5585delinsGC	XP_011513758.1:n.-17-5586_-17-5585delinsGC
XM_011515453.2:c.-17-5586_-17-5585delinsGC	XP_011513755.1:n.-17-5586_-17-5585delinsGC
XM_011515455.2:c.-17-5586_-17-5585delinsGC	XP_011513757.1:n.-17-5586_-17-5585delinsGC
XM_011515456.2:c.-17-5586_-17-5585delinsGC	XP_011513758.1:n.-17-5586_-17-5585delinsGC
XM_017012442.1:c.-17-5586_-17-5585delinsGC	XP_016867931.1:n.-17-5586_-17-5585delinsGC
XM_017012444.1:c.-17-5586_-17-5585delinsGC	XP_016867933.1:n.-17-5586_-17-5585delinsGC
XM_017012445.1:c.-17-5586_-17-5585delinsGC	XP_016867934.1:n.-17-5586_-17-5585delinsGC
XM_017012446.1:c.-17-5586_-17-5585delinsGC	XP_016867935.1:n.-17-5586_-17-5585delinsGC
XM_017012447.1:c.-17-5586_-17-5585delinsGC	XP_016867936.1:n.-17-5586_-17-5585delinsGC
XM_017012448.1:c.-17-5586_-17-5585delinsGC	XP_016867937.1:n.-17-5586_-17-5585delinsGC
XM_024446838.1:c.-17-5586_-17-5585delinsGC	XP_024302606.1:n.-17-5586_-17-5585delinsGC
NM_020156.5:c.-17-5586_-17-5585delinsGC MANE Select	NP_064541.1:n.-17-5586_-17-5585delinsGC