Canonical Allele Identifier: CA2627716076

Gene: SPRED1

Linked Data

• gnomAD v4: 15-38349578-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38349578T>A , CM000677.2:g.38349578T>A	GRCh38
NC_000015.9:g.38641779T>A , CM000677.1:g.38641779T>A	GRCh37
NC_000015.8:g.36429071T>A	NCBI36
NG_008980.1:g.101728T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.684+55T>A MANE Select	ENSP00000299084.4:n.684+55T>A
ENST00000299084.8:c.684+55T>A	ENSP00000299084.4:n.684+55T>A
NM_152594.2:c.684+55T>A	NP_689807.1:n.684+55T>A
XM_005254202.2:c.720+55T>A	XP_005254259.1:n.720+55T>A
XM_005254203.3:c.462+55T>A	XP_005254260.1:n.462+55T>A
XM_011521288.1:c.621+55T>A	XP_011519590.1:n.621+55T>A
XM_011521289.1:c.621+55T>A	XP_011519591.1:n.621+55T>A
XM_011521290.1:c.621+55T>A	XP_011519592.1:n.621+55T>A
XM_005254202.3:c.720+55T>A	XP_005254259.1:n.720+55T>A
XM_011521289.3:c.621+55T>A	XP_011519591.1:n.621+55T>A
NM_152594.3:c.684+55T>A MANE Select	NP_689807.1:n.684+55T>A