Canonical Allele Identifier: CA1259891267
Gene: MCEE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71124313G= , CM000664.2:g.71124313G= GRCh38
NC_000002.11:g.71351443G= , CM000664.1:g.71351443G= GRCh37
NC_000002.10:g.71204951G= NCBI36
NG_008977.1:g.10952C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000244217.6:c.271C= MANE Select ENSP00000244217.5:p.Leu91=
ENST00000244217.5:c.271C= ENSP00000244217.5:p.Leu91=
ENST00000413592.5:c.84+55C= ENSP00000391140.1:n.84+55C=
ENST00000486135.1:c.-15C= ENSP00000441569.1:n.-15C=
ENST00000494660.6:c.-15C= ENSP00000437361.1:n.-15C=
NM_032601.3:c.271C= NP_115990.3:p.Leu91=
XM_005264613.2:c.216+55C= XP_005264670.1:n.216+55C=
XR_939729.1:n.340C=
XR_939729.2:n.340C=
NM_032601.4:c.271C= MANE Select NP_115990.3:p.Leu91=