Canonical Allele Identifier: CA2791288785

Gene: SLC35C1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45805799_45805800del , CM000673.2:g.45805799_45805800del	GRCh38
NC_000011.9:g.45827350_45827351del , CM000673.1:g.45827350_45827351del	GRCh37
NC_000011.8:g.45783926_45783927del	NCBI36
NG_009875.1:g.6728_6729del , LRG_107:g.6728_6729del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526817.2:c.-31-11_-31-10del	ENSP00000432145.2:n.-31-11_-31-10del
ENST00000314134.4:c.-3_-2del MANE Select	ENSP00000313318.3:n.-3_-2del
ENST00000314134.3:c.-3_-2del	ENSP00000313318.3:n.-3_-2del
ENST00000442528.2:c.-31-11_-31-10del	ENSP00000412408.2:n.-31-11_-31-10del
ENST00000526817.1:c.-31-11_-31-10del	ENSP00000432145.1:n.-31-11_-31-10del
ENST00000530471.1:c.-31-11_-31-10del	ENSP00000432669.1:n.-31-11_-31-10del
NM_001145265.1:c.-31-11_-31-10del	NP_001138737.1:n.-31-11_-31-10del
NM_001145266.1:c.-31-11_-31-10del	NP_001138738.1:n.-31-11_-31-10del
NM_018389.4:c.-3_-2del , LRG_107t1:c.-3_-2del	NP_060859.4:n.-3_-2del
XM_011520203.1:c.-3_-2del	XP_011518505.1:n.-3_-2del
XM_011520203.3:c.-3_-2del	XP_011518505.1:n.-3_-2del
NM_001145265.2:c.-31-11_-31-10del	NP_001138737.1:n.-31-11_-31-10del
NM_018389.5:c.-3_-2del MANE Select	NP_060859.4:n.-3_-2del