Canonical Allele Identifier: CA2627715280

Gene: SPRED1

Linked Data

• gnomAD v4: 15-38322162-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38322162C>A , CM000677.2:g.38322162C>A	GRCh38
NC_000015.9:g.38614363C>A , CM000677.1:g.38614363C>A	GRCh37
NC_000015.8:g.36401655C>A	NCBI36
NG_008980.1:g.74312C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000299084.9:c.208-79C>A MANE Select	ENSP00000299084.4:n.208-79C>A
ENST00000299084.8:c.208-79C>A	ENSP00000299084.4:n.208-79C>A
ENST00000561205.1:n.546-79C>A
ENST00000561317.1:c.145-79C>A	ENSP00000453680.1:n.145-79C>A
NM_152594.2:c.208-79C>A	NP_689807.1:n.208-79C>A
XM_005254202.2:c.244-79C>A	XP_005254259.1:n.244-79C>A
XM_005254203.3:c.-15-79C>A	XP_005254260.1:n.-15-79C>A
XM_011521288.1:c.145-79C>A	XP_011519590.1:n.145-79C>A
XM_011521289.1:c.145-79C>A	XP_011519591.1:n.145-79C>A
XM_011521290.1:c.145-79C>A	XP_011519592.1:n.145-79C>A
XM_005254202.3:c.244-79C>A	XP_005254259.1:n.244-79C>A
XM_011521289.3:c.145-79C>A	XP_011519591.1:n.145-79C>A
NM_152594.3:c.208-79C>A MANE Select	NP_689807.1:n.208-79C>A