Canonical Allele Identifier: CA2627714184
Gene: SPRED1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38252975G>T , CM000677.2:g.38252975G>T GRCh38
NC_000015.9:g.38545176G>T , CM000677.1:g.38545176G>T GRCh37
NC_000015.8:g.36332468G>T NCBI36
NG_008980.1:g.5125G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.-211G>T MANE Select ENSP00000299084.4:n.-211G>T
ENST00000299084.8:c.-211G>T ENSP00000299084.4:n.-211G>T
ENST00000561205.1:n.128G>T
NM_152594.2:c.-211G>T NP_689807.1:n.-211G>T
XM_005254202.2:c.-211G>T XP_005254259.1:n.-211G>T
XM_005254203.3:c.-258G>T XP_005254260.1:n.-258G>T
XM_005254202.3:c.-211G>T XP_005254259.1:n.-211G>T
XR_001751484.1:n.87+592C>A
NM_152594.3:c.-211G>T MANE Select NP_689807.1:n.-211G>T