Canonical Allele Identifier: CA2170765552
Gene: SPRED1 HGNC NCBI

Linked Data

dbSNP Id: rs1894010585
gnomAD v4: 15-38252975-G-A
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Genomic Alleles

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

Transcript Alleles

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