Canonical Allele Identifier: CA2627715268

Gene: SPRED1

Linked Data

• gnomAD v4: 15-38322137-TCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38322138_38322139del , CM000677.2:g.38322138_38322139del	GRCh38
NC_000015.9:g.38614339_38614340del , CM000677.1:g.38614339_38614340del	GRCh37
NC_000015.8:g.36401631_36401632del	NCBI36
NG_008980.1:g.74288_74289del

Transcript Alleles

HGVS	Amino-acid change
ENST00000299084.9:c.208-103_208-102del MANE Select	ENSP00000299084.4:n.208-103_208-102del
ENST00000299084.8:c.208-103_208-102del	ENSP00000299084.4:n.208-103_208-102del
ENST00000561205.1:n.546-103_546-102del
ENST00000561317.1:c.145-103_145-102del	ENSP00000453680.1:n.145-103_145-102del
NM_152594.2:c.208-103_208-102del	NP_689807.1:n.208-103_208-102del
XM_005254202.2:c.244-103_244-102del	XP_005254259.1:n.244-103_244-102del
XM_005254203.3:c.-15-103_-15-102del	XP_005254260.1:n.-15-103_-15-102del
XM_011521288.1:c.145-103_145-102del	XP_011519590.1:n.145-103_145-102del
XM_011521289.1:c.145-103_145-102del	XP_011519591.1:n.145-103_145-102del
XM_011521290.1:c.145-103_145-102del	XP_011519592.1:n.145-103_145-102del
XM_005254202.3:c.244-103_244-102del	XP_005254259.1:n.244-103_244-102del
XM_011521289.3:c.145-103_145-102del	XP_011519591.1:n.145-103_145-102del
NM_152594.3:c.208-103_208-102del MANE Select	NP_689807.1:n.208-103_208-102del