Canonical Allele Identifier: CA1257213489

Gene: SPRED2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.65382094_65382095delinsCT , CM000664.2:g.65382094_65382095delinsCT	GRCh38
NC_000002.11:g.65609228_65609229delinsCT , CM000664.1:g.65609228_65609229delinsCT	GRCh37
NC_000002.10:g.65462732_65462733delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356388.9:c.27-37199_27-37198delinsAG MANE Select	ENSP00000348753.4:n.27-37199_27-37198delinsAG
ENST00000356388.8:c.27-37199_27-37198delinsAG	ENSP00000348753.4:n.27-37199_27-37198delinsAG
ENST00000440972.1:c.27-37199_27-37198delinsAG	ENSP00000406481.1:n.27-37199_27-37198delinsAG
NM_181784.2:c.27-37199_27-37198delinsAG	NP_861449.2:n.27-37199_27-37198delinsAG
XM_005264200.3:c.27-37199_27-37198delinsAG	XP_005264257.2:n.27-37199_27-37198delinsAG
XM_005264202.3:c.27-37199_27-37198delinsAG	XP_005264259.1:n.27-37199_27-37198delinsAG
XM_006711966.1:c.27-37199_27-37198delinsAG	XP_006712029.1:n.27-37199_27-37198delinsAG
XM_005264200.5:c.27-37199_27-37198delinsAG	XP_005264257.2:n.27-37199_27-37198delinsAG
XM_005264202.5:c.27-37199_27-37198delinsAG	XP_005264259.1:n.27-37199_27-37198delinsAG
NM_181784.3:c.27-37199_27-37198delinsAG MANE Select	NP_861449.2:n.27-37199_27-37198delinsAG