Canonical Allele Identifier: CA2170765644
Gene: SPRED1 HGNC NCBI

Linked Data

dbSNP Id: rs1894012442

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38253048C>G , CM000677.2:g.38253048C>G GRCh38
NC_000015.9:g.38545249C>G , CM000677.1:g.38545249C>G GRCh37
NC_000015.8:g.36332541C>G NCBI36
NG_008980.1:g.5198C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000299084.9:c.-138C>G MANE Select ENSP00000299084.4:n.-138C>G
ENST00000299084.8:c.-138C>G ENSP00000299084.4:n.-138C>G
ENST00000561205.1:n.201C>G
NM_152594.2:c.-138C>G NP_689807.1:n.-138C>G
XM_005254202.2:c.-138C>G XP_005254259.1:n.-138C>G
XM_005254203.3:c.-185C>G XP_005254260.1:n.-185C>G
XM_005254202.3:c.-138C>G XP_005254259.1:n.-138C>G
XR_001751484.1:n.87+519G>C
NM_152594.3:c.-138C>G MANE Select NP_689807.1:n.-138C>G