Canonical Allele Identifier: CA712588239

Gene: SPRED1

Linked Data

• dbSNP Id: rs1451021355
• gnomAD v3: 15-38253060-T-C
• gnomAD v4: 15-38253060-T-C
• MyVariant Identifiers: chr15:g.38545261T>C (hg19) ; chr15:g.38253060T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38253060T>C , CM000677.2:g.38253060T>C	GRCh38
NC_000015.9:g.38545261T>C , CM000677.1:g.38545261T>C	GRCh37
NC_000015.8:g.36332553T>C	NCBI36
NG_008980.1:g.5210T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.-126T>C MANE Select	ENSP00000299084.4:n.-126T>C
ENST00000299084.8:c.-126T>C	ENSP00000299084.4:n.-126T>C
ENST00000561205.1:n.213T>C
NM_152594.2:c.-126T>C	NP_689807.1:n.-126T>C
XM_005254202.2:c.-126T>C	XP_005254259.1:n.-126T>C
XM_005254203.3:c.-173T>C	XP_005254260.1:n.-173T>C
XM_005254202.3:c.-126T>C	XP_005254259.1:n.-126T>C
XR_001751484.1:n.87+507A>G
NM_152594.3:c.-126T>C MANE Select	NP_689807.1:n.-126T>C