Canonical Allele Identifier: CA2627714270
Gene: SPRED1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38253038C>T , CM000677.2:g.38253038C>T GRCh38
NC_000015.9:g.38545239C>T , CM000677.1:g.38545239C>T GRCh37
NC_000015.8:g.36332531C>T NCBI36
NG_008980.1:g.5188C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000299084.9:c.-148C>T MANE Select ENSP00000299084.4:n.-148C>T
ENST00000299084.8:c.-148C>T ENSP00000299084.4:n.-148C>T
ENST00000561205.1:n.191C>T
NM_152594.2:c.-148C>T NP_689807.1:n.-148C>T
XM_005254202.2:c.-148C>T XP_005254259.1:n.-148C>T
XM_005254203.3:c.-195C>T XP_005254260.1:n.-195C>T
XM_005254202.3:c.-148C>T XP_005254259.1:n.-148C>T
XR_001751484.1:n.87+529G>A
NM_152594.3:c.-148C>T MANE Select NP_689807.1:n.-148C>T