Canonical Allele Identifier: CA269293950
Gene: SPRED1 HGNC NCBI

Linked Data

dbSNP Id: rs1023546514
MyVariant Identifiers: chr15:g.38648688T>C (hg19) chr15:g.38356487T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38356487T>C , CM000677.2:g.38356487T>C GRCh38
NC_000015.9:g.38648688T>C , CM000677.1:g.38648688T>C GRCh37
NC_000015.8:g.36435980T>C NCBI36
NG_008980.1:g.108637T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000299084.9:c.*4823T>C MANE Select ENSP00000299084.4:n.*4823T>C
ENST00000299084.8:c.*4823T>C ENSP00000299084.4:n.*4823T>C
NM_152594.2:c.*4823T>C NP_689807.1:n.*4823T>C
XM_005254202.3:c.*4823T>C XP_005254259.1:n.*4823T>C
XM_011521289.3:c.*4823T>C XP_011519591.1:n.*4823T>C
NM_152594.3:c.*4823T>C MANE Select NP_689807.1:n.*4823T>C
Search 100 bp 5'
Search 100 bp 3'