Canonical Allele Identifier: CA1259891243
Gene: MCEE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71124243T= , CM000664.2:g.71124243T= GRCh38
NC_000002.11:g.71351373T= , CM000664.1:g.71351373T= GRCh37
NC_000002.10:g.71204881T= NCBI36
NG_008977.1:g.11022A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000244217.6:c.341A= MANE Select ENSP00000244217.5:p.Lys114=
ENST00000244217.5:c.341A= ENSP00000244217.5:p.Lys114=
ENST00000413592.5:c.84+125A= ENSP00000391140.1:n.84+125A=
ENST00000486135.1:c.56A= ENSP00000441569.1:p.Lys19=
ENST00000494660.6:c.56A= ENSP00000437361.1:p.Lys19=
NM_032601.3:c.341A= NP_115990.3:p.Lys114=
XM_005264613.2:c.216+125A= XP_005264670.1:n.216+125A=
XR_939729.1:n.410A=
XR_939729.2:n.410A=
NM_032601.4:c.341A= MANE Select NP_115990.3:p.Lys114=