Canonical Allele Identifier: CA617500581

Gene: SPRED1

Linked Data

• dbSNP Id: rs1387485506
• gnomAD v2: 15-38591484-A-C
• gnomAD v3: 15-38299283-A-C
• gnomAD v4: 15-38299283-A-C
• MyVariant Identifiers: chr15:g.38591484A>C (hg19) ; chr15:g.38299283A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38299283A>C , CM000677.2:g.38299283A>C	GRCh38
NC_000015.9:g.38591484A>C , CM000677.1:g.38591484A>C	GRCh37
NC_000015.8:g.36378776A>C	NCBI36
NG_008980.1:g.51433A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000299084.9:c.33-90A>C MANE Select	ENSP00000299084.4:n.33-90A>C
ENST00000299084.8:c.33-90A>C	ENSP00000299084.4:n.33-90A>C
ENST00000561205.1:n.371-90A>C
ENST00000561317.1:c.-31-90A>C	ENSP00000453680.1:n.-31-90A>C
NM_152594.2:c.33-90A>C	NP_689807.1:n.33-90A>C
XM_005254202.2:c.69-90A>C	XP_005254259.1:n.69-90A>C
XM_005254203.3:c.-15-22958A>C	XP_005254260.1:n.-15-22958A>C
XM_011521288.1:c.-31-90A>C	XP_011519590.1:n.-31-90A>C
XM_011521289.1:c.-31-90A>C	XP_011519591.1:n.-31-90A>C
XM_011521290.1:c.-31-90A>C	XP_011519592.1:n.-31-90A>C
XM_005254202.3:c.69-90A>C	XP_005254259.1:n.69-90A>C
XM_011521289.3:c.-31-90A>C	XP_011519591.1:n.-31-90A>C
NM_152594.3:c.33-90A>C MANE Select	NP_689807.1:n.33-90A>C