Canonical Allele Identifier: CA1259891388
Gene: MCEE HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71124589G= , CM000664.2:g.71124589G= GRCh38
NC_000002.11:g.71351719G= , CM000664.1:g.71351719G= GRCh37
NC_000002.10:g.71205227G= NCBI36
NG_008977.1:g.10676C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000244217.6:c.41-46C= MANE Select ENSP00000244217.5:n.41-46C=
ENST00000244217.5:c.41-46C= ENSP00000244217.5:n.41-46C=
ENST00000486135.1:c.-245-46C= ENSP00000441569.1:n.-245-46C=
ENST00000494660.6:c.-245-46C= ENSP00000437361.1:n.-245-46C=
NM_032601.3:c.41-46C= NP_115990.3:n.41-46C=
XM_005264613.2:c.41-46C= XP_005264670.1:n.41-46C=
XR_939729.1:n.110-46C=
XR_939729.2:n.110-46C=
NM_032601.4:c.41-46C= MANE Select NP_115990.3:n.41-46C=
Search 100 bp 5'
Search 100 bp 3'