Canonical Allele Identifier: CA1139981751

Gene: ECE1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21220008G= , CM000663.2:g.21220008G=	GRCh38
NC_000001.10:g.21546501G= , CM000663.1:g.21546501G=	GRCh37
NC_000001.9:g.21419088G=	NCBI36
NG_013008.1:g.130534C=
NG_013008.2:g.130534C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374893.11:c.2260C= MANE Select	ENSP00000364028.6:p.Arg754=
ENST00000649812.1:c.2212C=	ENSP00000497333.1:p.Arg738=
ENST00000264205.10:c.2251C=	ENSP00000264205.6:p.Arg751=
ENST00000357071.8:c.2224C=	ENSP00000349581.4:p.Arg742=
ENST00000374893.10:c.2260C=	ENSP00000364028.6:p.Arg754=
ENST00000415912.6:c.2212C=	ENSP00000405088.2:p.Arg738=
ENST00000436918.6:c.2164C=	ENSP00000388439.2:p.Arg722=
ENST00000531334.1:n.459C=
NM_001113347.1:c.2224C=	NP_001106818.1:p.Arg742=
NM_001113348.1:c.2212C=	NP_001106819.1:p.Arg738=
NM_001113349.1:c.2251C=	NP_001106820.1:p.Arg751=
NM_001397.2:c.2260C=	NP_001388.1:p.Arg754=
XM_006710398.1:c.2209C=	XP_006710461.1:p.Arg737=
XM_011540872.1:c.2284C=	XP_011539174.1:p.Arg762=
XM_011540873.1:c.2209C=	XP_011539175.1:p.Arg737=
XM_006710398.2:c.2209C=	XP_006710461.1:p.Arg737=
XM_011540872.2:c.2284C=	XP_011539174.1:p.Arg762=
XM_011540873.2:c.2209C=	XP_011539175.1:p.Arg737=
NM_001397.3:c.2260C= MANE Select	NP_001388.1:p.Arg754=
NM_001113347.2:c.2224C=	NP_001106818.1:p.Arg742=
NM_001113348.2:c.2212C=	NP_001106819.1:p.Arg738=
NM_001113349.2:c.2251C=	NP_001106820.1:p.Arg751=