Canonical Allele Identifier: CA712580084
Gene: SPRED1 HGNC NCBI

Linked Data

dbSNP Id: rs1476689139
gnomAD v3: 15-38356546-A-T
gnomAD v4: 15-38356546-A-T
MyVariant Identifiers: chr15:g.38648747A>T (hg19) chr15:g.38356546A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38356546A>T , CM000677.2:g.38356546A>T GRCh38
NC_000015.9:g.38648747A>T , CM000677.1:g.38648747A>T GRCh37
NC_000015.8:g.36436039A>T NCBI36
NG_008980.1:g.108696A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000299084.9:c.*4882A>T MANE Select ENSP00000299084.4:n.*4882A>T
ENST00000299084.8:c.*4882A>T ENSP00000299084.4:n.*4882A>T
NM_152594.2:c.*4882A>T NP_689807.1:n.*4882A>T
XM_005254202.3:c.*4882A>T XP_005254259.1:n.*4882A>T
XM_011521289.3:c.*4882A>T XP_011519591.1:n.*4882A>T
NM_152594.3:c.*4882A>T MANE Select NP_689807.1:n.*4882A>T
Search 100 bp 5'
Search 100 bp 3'