Canonical Allele Identifier: CA2575673106
Gene: SPRED1 HGNC NCBI

Linked Data

gnomAD v4: 15-38253110-T-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38253110T>C , CM000677.2:g.38253110T>C GRCh38
NC_000015.9:g.38545311T>C , CM000677.1:g.38545311T>C GRCh37
NC_000015.8:g.36332603T>C NCBI36
NG_008980.1:g.5260T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.-76T>C MANE Select ENSP00000299084.4:n.-76T>C
ENST00000299084.8:c.-76T>C ENSP00000299084.4:n.-76T>C
ENST00000561205.1:n.263T>C
NM_152594.2:c.-76T>C NP_689807.1:n.-76T>C
XM_005254202.2:c.-76T>C XP_005254259.1:n.-76T>C
XM_005254203.3:c.-123T>C XP_005254260.1:n.-123T>C
XM_005254202.3:c.-76T>C XP_005254259.1:n.-76T>C
XR_001751484.1:n.87+457A>G
NM_152594.3:c.-76T>C MANE Select NP_689807.1:n.-76T>C
Search 100 bp 5'
Search 100 bp 3'