Canonical Allele Identifier: CA2170814988
Gene: SPRED1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38356546A= , CM000677.2:g.38356546A= GRCh38
NC_000015.9:g.38648747A= , CM000677.1:g.38648747A= GRCh37
NC_000015.8:g.36436039A= NCBI36
NG_008980.1:g.108696A=

Transcript Alleles

HGVS Amino-acid change
ENST00000299084.9:c.*4882A= MANE Select ENSP00000299084.4:n.*4882A=
ENST00000299084.8:c.*4882A= ENSP00000299084.4:n.*4882A=
NM_152594.2:c.*4882A= NP_689807.1:n.*4882A=
XM_005254202.3:c.*4882A= XP_005254259.1:n.*4882A=
XM_011521289.3:c.*4882A= XP_011519591.1:n.*4882A=
NM_152594.3:c.*4882A= MANE Select NP_689807.1:n.*4882A=