Canonical Allele Identifier: CA2170814953

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38356440C= , CM000677.2:g.38356440C=	GRCh38
NC_000015.9:g.38648641C= , CM000677.1:g.38648641C=	GRCh37
NC_000015.8:g.36435933C=	NCBI36
NG_008980.1:g.108590C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000299084.9:c.*4776C= MANE Select	ENSP00000299084.4:n.*4776C=
ENST00000299084.8:c.*4776C=	ENSP00000299084.4:n.*4776C=
NM_152594.2:c.*4776C=	NP_689807.1:n.*4776C=
XM_005254202.2:c.*4776C=	XP_005254259.1:n.*4776C=
XM_005254203.3:c.*4776C=	XP_005254260.1:n.*4776C=
XM_011521288.1:c.*4776C=	XP_011519590.1:n.*4776C=
XM_011521289.1:c.*4776C=	XP_011519591.1:n.*4776C=
XM_011521290.1:c.*4776C=	XP_011519592.1:n.*4776C=
XM_005254202.3:c.*4776C=	XP_005254259.1:n.*4776C=
XM_011521289.3:c.*4776C=	XP_011519591.1:n.*4776C=
NM_152594.3:c.*4776C= MANE Select	NP_689807.1:n.*4776C=