Canonical Allele Identifier: CA2170814968
Gene: SPRED1 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000299084.9:c.*4823T= MANE Select ENSP00000299084.4:n.*4823T=
ENST00000299084.8:c.*4823T= ENSP00000299084.4:n.*4823T=
NM_152594.2:c.*4823T= NP_689807.1:n.*4823T=
XM_005254202.3:c.*4823T= XP_005254259.1:n.*4823T=
XM_011521289.3:c.*4823T= XP_011519591.1:n.*4823T=
NM_152594.3:c.*4823T= MANE Select NP_689807.1:n.*4823T=