Canonical Allele Identifier: CA1616492909

Gene: MRS2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24420316G= , CM000668.2:g.24420316G=	GRCh38
NC_000006.11:g.24420544G= , CM000668.1:g.24420544G=	GRCh37
NC_000006.10:g.24528523G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_020662.4:c.1107+1738G= MANE Select	NP_065713.1:n.1107+1738G=
ENST00000378386.8:c.1107+1738G= MANE Select	ENSP00000367637.3:n.1107+1738G=
NM_001286264.1:c.1116+1738G=	NP_001273193.1:n.1116+1738G=
NM_001286264.2:c.1116+1738G=	NP_001273193.1:n.1116+1738G=
NM_001286265.1:c.1107+1738G=	NP_001273194.1:n.1107+1738G=
NM_001286265.2:c.1107+1738G=	NP_001273194.1:n.1107+1738G=
NM_001286266.1:c.957+1738G=	NP_001273195.1:n.957+1738G=
NM_001286266.2:c.957+1738G=	NP_001273195.1:n.957+1738G=
NM_020662.3:c.1107+1738G=	NP_065713.1:n.1107+1738G=
NR_104423.1:n.1189+1738G=
NR_104423.2:n.1161+1738G=
ENST00000274747.11:c.957+1738G=	ENSP00000274747.8:n.957+1738G=
ENST00000378353.5:c.1107+1738G=	ENSP00000367604.1:n.1107+1738G=
ENST00000378386.7:c.1107+1738G=	ENSP00000367637.3:n.1107+1738G=
ENST00000443868.6:c.1116+1738G=	ENSP00000399585.2:n.1116+1738G=
XM_005249242.1:c.1107+1738G=	XP_005249299.1:n.1107+1738G=
XM_005249242.2:c.1107+1738G=	XP_005249299.1:n.1107+1738G=
XR_001743533.2:n.1308+1738G=