Canonical Allele Identifier: CA391933902
Gene: SPRED1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38299410C>G , CM000677.2:g.38299410C>G GRCh38
NC_000015.9:g.38591611C>G , CM000677.1:g.38591611C>G GRCh37
NC_000015.8:g.36378903C>G NCBI36
NG_008980.1:g.51560C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.70C>G MANE Select ENSP00000299084.4:p.Arg24Gly
ENST00000299084.8:c.70C>G ENSP00000299084.4:p.Arg24Gly
ENST00000561205.1:n.408C>G
ENST00000561317.1:c.7C>G ENSP00000453680.1:p.Arg3Gly
NM_152594.2:c.70C>G NP_689807.1:p.Arg24Gly
XM_005254202.2:c.106C>G XP_005254259.1:p.Arg36Gly
XM_005254203.3:c.-15-22831C>G XP_005254260.1:n.-15-22831C>G
XM_011521288.1:c.7C>G XP_011519590.1:p.Arg3Gly
XM_011521289.1:c.7C>G XP_011519591.1:p.Arg3Gly
XM_011521290.1:c.7C>G XP_011519592.1:p.Arg3Gly
XM_005254202.3:c.106C>G XP_005254259.1:p.Arg36Gly
XM_011521289.3:c.7C>G XP_011519591.1:p.Arg3Gly
NM_152594.3:c.70C>G MANE Select NP_689807.1:p.Arg24Gly