Canonical Allele Identifier: CA617505696

Gene: SPRED1

Linked Data

• dbSNP Id: rs1297150228
• gnomAD v2: 15-38641576-A-G
• gnomAD v4: 15-38349375-A-G
• MyVariant Identifiers: chr15:g.38641576A>G (hg19) ; chr15:g.38349375A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38349375A>G , CM000677.2:g.38349375A>G	GRCh38
NC_000015.9:g.38641576A>G , CM000677.1:g.38641576A>G	GRCh37
NC_000015.8:g.36428868A>G	NCBI36
NG_008980.1:g.101525A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.583-47A>G MANE Select	ENSP00000299084.4:n.583-47A>G
ENST00000299084.8:c.583-47A>G	ENSP00000299084.4:n.583-47A>G
NM_152594.2:c.583-47A>G	NP_689807.1:n.583-47A>G
XM_005254202.2:c.619-47A>G	XP_005254259.1:n.619-47A>G
XM_005254203.3:c.361-47A>G	XP_005254260.1:n.361-47A>G
XM_011521288.1:c.520-47A>G	XP_011519590.1:n.520-47A>G
XM_011521289.1:c.520-47A>G	XP_011519591.1:n.520-47A>G
XM_011521290.1:c.520-47A>G	XP_011519592.1:n.520-47A>G
XM_005254202.3:c.619-47A>G	XP_005254259.1:n.619-47A>G
XM_011521289.3:c.520-47A>G	XP_011519591.1:n.520-47A>G
NM_152594.3:c.583-47A>G MANE Select	NP_689807.1:n.583-47A>G