Canonical Allele Identifier: CA2730800030
Gene: SPRED1 HGNC NCBI

Linked Data

dbSNP Id: rs2141020184
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38356526T>C , CM000677.2:g.38356526T>C GRCh38
NC_000015.9:g.38648727T>C , CM000677.1:g.38648727T>C GRCh37
NC_000015.8:g.36436019T>C NCBI36
NG_008980.1:g.108676T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000299084.9:c.*4862T>C MANE Select ENSP00000299084.4:n.*4862T>C
ENST00000299084.8:c.*4862T>C ENSP00000299084.4:n.*4862T>C
NM_152594.2:c.*4862T>C NP_689807.1:n.*4862T>C
XM_005254202.3:c.*4862T>C XP_005254259.1:n.*4862T>C
XM_011521289.3:c.*4862T>C XP_011519591.1:n.*4862T>C
NM_152594.3:c.*4862T>C MANE Select NP_689807.1:n.*4862T>C
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