Canonical Allele Identifier: CA2696040895
Gene: SLC35D1 HGNC NCBI

Linked Data

dbSNP Id: rs2102385375

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67054102A>G , CM000663.2:g.67054102A>G GRCh38
NC_000001.10:g.67519785A>G , CM000663.1:g.67519785A>G GRCh37
NC_000001.9:g.67292373A>G NCBI36
NG_012933.1:g.5296T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.-89T>C MANE Select ENSP00000235345.5:n.-89T>C
NM_015139.2:c.-89T>C NP_055954.1:n.-89T>C
XM_006710478.1:c.-89T>C XP_006710541.1:n.-89T>C
XM_011541070.1:c.-89T>C XP_011539372.1:n.-89T>C
XM_006710478.2:c.-89T>C XP_006710541.1:n.-89T>C
XM_011541070.2:c.-89T>C XP_011539372.1:n.-89T>C
XR_001737057.2:n.322T>C
XR_001737058.2:n.315T>C
NM_015139.3:c.-89T>C MANE Select NP_055954.1:n.-89T>C