Canonical Allele Identifier: CA1139995839

Gene: MEF2D

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156486509C= , CM000663.2:g.156486509C=	GRCh38
NC_000001.10:g.156456301C= , CM000663.1:g.156456301C=	GRCh37
NC_000001.9:g.154722925C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_005920.4:c.-138-3079G= MANE Select	NP_005911.1:n.-138-3079G=
ENST00000348159.9:c.-138-3079G= MANE Select	ENSP00000271555.5:n.-138-3079G=
NM_001271629.1:c.-126-3091G=	NP_001258558.1:n.-126-3091G=
NM_001271629.2:c.-126-3091G=	NP_001258558.1:n.-126-3091G=
NM_005920.3:c.-138-3079G=	NP_005911.1:n.-138-3079G=
ENST00000348159.8:c.-138-3079G=	ENSP00000271555.5:n.-138-3079G=
ENST00000360595.7:c.-126-3091G=	ENSP00000353803.3:n.-126-3091G=
ENST00000368240.6:c.-138-3079G=	ENSP00000357223.3:n.-138-3079G=
ENST00000475587.2:c.-138-3079G=	ENSP00000477413.1:n.-138-3079G=
ENST00000489057.1:c.-138-3079G=	ENSP00000477124.1:n.-138-3079G=
XM_005245169.3:c.-126-3091G=	XP_005245226.1:n.-126-3091G=
XM_005245169.4:c.-126-3091G=	XP_005245226.1:n.-126-3091G=
XM_005245170.2:c.-138-3079G=	XP_005245227.1:n.-138-3079G=
XM_005245170.3:c.-138-3079G=	XP_005245227.1:n.-138-3079G=
XM_006711330.2:c.-138-3079G=	XP_006711393.1:n.-138-3079G=
XM_006711330.3:c.-138-3079G=	XP_006711393.1:n.-138-3079G=
XM_006711332.2:c.-138-3079G=	XP_006711395.1:n.-138-3079G=
XM_006711332.3:c.-138-3079G=	XP_006711395.1:n.-138-3079G=
XM_006711333.2:c.-138-3079G=	XP_006711396.1:n.-138-3079G=
XM_006711334.2:c.-138-3079G=	XP_006711397.1:n.-138-3079G=
XM_006711334.3:c.-138-3079G=	XP_006711397.1:n.-138-3079G=
XM_011509569.1:c.-138-3079G=	XP_011507871.1:n.-138-3079G=
XM_011509569.3:c.-138-3079G=	XP_011507871.1:n.-138-3079G=
XM_011509570.1:c.-138-3079G=	XP_011507872.1:n.-138-3079G=
XM_017001314.1:c.-138-3079G=	XP_016856803.1:n.-138-3079G=
XM_017001315.1:c.-138-3079G=	XP_016856804.1:n.-138-3079G=
XR_001737184.1:n.353-3079G=