Canonical Allele Identifier: CA2627717233

Gene: SPRED1

Linked Data

• gnomAD v4: 15-38355529-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38355529C>A , CM000677.2:g.38355529C>A	GRCh38
NC_000015.9:g.38647730C>A , CM000677.1:g.38647730C>A	GRCh37
NC_000015.8:g.36435022C>A	NCBI36
NG_008980.1:g.107679C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000299084.9:c.*3865C>A MANE Select	ENSP00000299084.4:n.*3865C>A
ENST00000299084.8:c.*3865C>A	ENSP00000299084.4:n.*3865C>A
NM_152594.2:c.*3865C>A	NP_689807.1:n.*3865C>A
XM_005254202.2:c.*3865C>A	XP_005254259.1:n.*3865C>A
XM_005254203.3:c.*3865C>A	XP_005254260.1:n.*3865C>A
XM_011521288.1:c.*3865C>A	XP_011519590.1:n.*3865C>A
XM_011521289.1:c.*3865C>A	XP_011519591.1:n.*3865C>A
XM_011521290.1:c.*3865C>A	XP_011519592.1:n.*3865C>A
XM_005254202.3:c.*3865C>A	XP_005254259.1:n.*3865C>A
XM_011521289.3:c.*3865C>A	XP_011519591.1:n.*3865C>A
NM_152594.3:c.*3865C>A MANE Select	NP_689807.1:n.*3865C>A