Canonical Allele Identifier: CA2170814978
Gene: SPRED1 HGNC NCBI

Linked Data

dbSNP Id: rs1888624989
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38356509A>G , CM000677.2:g.38356509A>G GRCh38
NC_000015.9:g.38648710A>G , CM000677.1:g.38648710A>G GRCh37
NC_000015.8:g.36436002A>G NCBI36
NG_008980.1:g.108659A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000299084.9:c.*4845A>G MANE Select ENSP00000299084.4:n.*4845A>G
ENST00000299084.8:c.*4845A>G ENSP00000299084.4:n.*4845A>G
NM_152594.2:c.*4845A>G NP_689807.1:n.*4845A>G
XM_005254202.3:c.*4845A>G XP_005254259.1:n.*4845A>G
XM_011521289.3:c.*4845A>G XP_011519591.1:n.*4845A>G
NM_152594.3:c.*4845A>G MANE Select NP_689807.1:n.*4845A>G
Search 100 bp 5'
Search 100 bp 3'