Canonical Allele Identifier: CA269282668

Gene: SPRED1

Linked Data

• dbSNP Id: rs934247696
• MyVariant Identifiers: chr15:g.38545484A>G (hg19) ; chr15:g.38253283A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38253283A>G , CM000677.2:g.38253283A>G	GRCh38
NC_000015.9:g.38545484A>G , CM000677.1:g.38545484A>G	GRCh37
NC_000015.8:g.36332776A>G	NCBI36
NG_008980.1:g.5433A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.32+66A>G MANE Select	ENSP00000299084.4:n.32+66A>G
ENST00000299084.8:c.32+66A>G	ENSP00000299084.4:n.32+66A>G
ENST00000561205.1:n.370+66A>G
ENST00000561317.1:c.-96+66A>G	ENSP00000453680.1:n.-96+66A>G
NM_152594.2:c.32+66A>G	NP_689807.1:n.32+66A>G
XM_005254202.2:c.32+66A>G	XP_005254259.1:n.32+66A>G
XM_005254203.3:c.-16+66A>G	XP_005254260.1:n.-16+66A>G
XM_005254202.3:c.32+66A>G	XP_005254259.1:n.32+66A>G
XR_001751484.1:n.87+284T>C
NM_152594.3:c.32+66A>G MANE Select	NP_689807.1:n.32+66A>G