Canonical Allele Identifier: CA2627714299
Gene: SPRED1 HGNC NCBI

Linked Data

gnomAD v4: 15-38253064-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38253064G>C , CM000677.2:g.38253064G>C GRCh38
NC_000015.9:g.38545265G>C , CM000677.1:g.38545265G>C GRCh37
NC_000015.8:g.36332557G>C NCBI36
NG_008980.1:g.5214G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000299084.9:c.-122G>C MANE Select ENSP00000299084.4:n.-122G>C
ENST00000299084.8:c.-122G>C ENSP00000299084.4:n.-122G>C
ENST00000561205.1:n.217G>C
NM_152594.2:c.-122G>C NP_689807.1:n.-122G>C
XM_005254202.2:c.-122G>C XP_005254259.1:n.-122G>C
XM_005254203.3:c.-169G>C XP_005254260.1:n.-169G>C
XM_005254202.3:c.-122G>C XP_005254259.1:n.-122G>C
XR_001751484.1:n.87+503C>G
NM_152594.3:c.-122G>C MANE Select NP_689807.1:n.-122G>C
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