Canonical Allele Identifier: CA1259891284
Gene: MCEE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71124353G= , CM000664.2:g.71124353G= GRCh38
NC_000002.11:g.71351483G= , CM000664.1:g.71351483G= GRCh37
NC_000002.10:g.71204991G= NCBI36
NG_008977.1:g.10912C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000244217.6:c.231C= MANE Select ENSP00000244217.5:p.Val77=
ENST00000244217.5:c.231C= ENSP00000244217.5:p.Val77=
ENST00000413592.5:c.84+15C= ENSP00000391140.1:n.84+15C=
ENST00000486135.1:c.-55C= ENSP00000441569.1:n.-55C=
ENST00000494660.6:c.-55C= ENSP00000437361.1:n.-55C=
NM_032601.3:c.231C= NP_115990.3:p.Val77=
XM_005264613.2:c.216+15C= XP_005264670.1:n.216+15C=
XR_939729.1:n.300C=
XR_939729.2:n.300C=
NM_032601.4:c.231C= MANE Select NP_115990.3:p.Val77=