Canonical Allele Identifier: CA146499381

Gene: SLC35F1

Linked Data

• dbSNP Id: rs918674318
• gnomAD v3: 6-118297666-TTATATAAGTTCTGAGAAATATATATTATA-T
• gnomAD v4: 6-118297666-TTATATAAGTTCTGAGAAATATATATTATA-T
• MyVariant Identifiers: chr6:g.118618830_118618858del (hg19) ; chr6:g.118297667_118297695del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.118297721_118297749del , CM000668.2:g.118297721_118297749del	GRCh38
NC_000006.11:g.118618884_118618912del , CM000668.1:g.118618884_118618912del	GRCh37
NC_000006.10:g.118725577_118725605del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000360388.9:c.1002+12383_1002+12411del MANE Select	ENSP00000353557.4:n.1002+12383_1002+12411...
ENST00000360388.8:c.1002+12383_1002+12411del	ENSP00000353557.4:n.1002+12383_1002+12411...
ENST00000621341.1:c.825+12383_825+12411del	ENSP00000484738.1:n.825+12383_825+12411de...
NM_001029858.3:c.1002+12383_1002+12411del	NP_001025029.2:n.1002+12383_1002+12411del...
XM_005266865.3:c.1002+12383_1002+12411del	XP_005266922.1:n.1002+12383_1002+12411del...
XR_942913.1:n.342-7185_342-7157del
XM_005266865.4:c.1002+12383_1002+12411del	XP_005266922.1:n.1002+12383_1002+12411del...
NM_001029858.4:c.1002+12383_1002+12411del MANE Select	NP_001025029.2:n.1002+12383_1002+12411del...