Canonical Allele Identifier: CA347185919
Gene: MCEE HGNC NCBI

Linked Data

gnomAD v4: 2-71124212-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71124212G>T , CM000664.2:g.71124212G>T GRCh38
NC_000002.11:g.71351342G>T , CM000664.1:g.71351342G>T GRCh37
NC_000002.10:g.71204850G>T NCBI36
NG_008977.1:g.11053C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000244217.6:c.372C>A MANE Select ENSP00000244217.5:p.Cys124Ter
ENST00000244217.5:c.372C>A ENSP00000244217.5:p.Cys124Ter
ENST00000413592.5:c.84+156C>A ENSP00000391140.1:n.84+156C>A
ENST00000486135.1:c.87C>A ENSP00000441569.1:p.Cys29Ter
ENST00000494660.6:c.87C>A ENSP00000437361.1:p.Cys29Ter
NM_032601.3:c.372C>A NP_115990.3:p.Cys124Ter
XM_005264613.2:c.216+156C>A XP_005264670.1:n.216+156C>A
XR_939729.1:n.441C>A
XR_939729.2:n.441C>A
NM_032601.4:c.372C>A MANE Select NP_115990.3:p.Cys124Ter