Canonical Allele Identifier: CA1172975803
Gene: SLC35D1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67053965_67053979delinsGGGCTTCTCCTTTAA , CM000663.2:g.67053965_67053979delinsGGGCTTCTCCTTTAA GRCh38
NC_000001.10:g.67519648_67519662delinsGGGCTTCTCCTTTAA , CM000663.1:g.67519648_67519662delinsGGGCTTCTCCTTTAA GRCh37
NC_000001.9:g.67292236_67292250delinsGGGCTTCTCCTTTAA NCBI36
NG_012933.1:g.5419_5433delinsTTAAAGGAGAAGCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.35_49delinsTTAAAGGAGAAGCCC MANE Select ENSP00000235345.5:p.Val12=
ENST00000235345.5:c.35_49delinsTTAAAGGAGAAGCCC ENSP00000235345.5:p.Val12=
NM_015139.2:c.35_49delinsTTAAAGGAGAAGCCC NP_055954.1:p.Val12=
XM_006710478.1:c.35_49delinsTTAAAGGAGAAGCCC XP_006710541.1:p.Val12=
XM_011541070.1:c.35_49delinsTTAAAGGAGAAGCCC XP_011539372.1:p.Val12=
XM_006710478.2:c.35_49delinsTTAAAGGAGAAGCCC XP_006710541.1:p.Val12=
XM_011541070.2:c.35_49delinsTTAAAGGAGAAGCCC XP_011539372.1:p.Val12=
XR_001737057.2:n.445_459delinsTTAAAGGAGAAGCCC
XR_001737058.2:n.438_452delinsTTAAAGGAGAAGCCC
NM_015139.3:c.35_49delinsTTAAAGGAGAAGCCC MANE Select NP_055954.1:p.Val12=