Canonical Allele Identifier: CA391933354
Gene: SPRED1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38351162C>T , CM000677.2:g.38351162C>T GRCh38
NC_000015.9:g.38643363C>T , CM000677.1:g.38643363C>T GRCh37
NC_000015.8:g.36430655C>T NCBI36
NG_008980.1:g.103312C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.833C>T MANE Select ENSP00000299084.4:p.Ser278Phe
ENST00000299084.8:c.833C>T ENSP00000299084.4:p.Ser278Phe
NM_152594.2:c.833C>T NP_689807.1:p.Ser278Phe
XM_005254202.2:c.869C>T XP_005254259.1:p.Ser290Phe
XM_005254203.3:c.611C>T XP_005254260.1:p.Ser204Phe
XM_011521288.1:c.770C>T XP_011519590.1:p.Ser257Phe
XM_011521289.1:c.770C>T XP_011519591.1:p.Ser257Phe
XM_011521290.1:c.770C>T XP_011519592.1:p.Ser257Phe
XM_005254202.3:c.869C>T XP_005254259.1:p.Ser290Phe
XM_011521289.3:c.770C>T XP_011519591.1:p.Ser257Phe
NM_152594.3:c.833C>T MANE Select NP_689807.1:p.Ser278Phe