Canonical Allele Identifier: CA347186315
Gene: MCEE HGNC NCBI

Linked Data

gnomAD v4: 2-71124242-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71124242T>G , CM000664.2:g.71124242T>G GRCh38
NC_000002.11:g.71351372T>G , CM000664.1:g.71351372T>G GRCh37
NC_000002.10:g.71204880T>G NCBI36
NG_008977.1:g.11023A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000244217.6:c.342A>C MANE Select ENSP00000244217.5:p.Lys114Asn
ENST00000244217.5:c.342A>C ENSP00000244217.5:p.Lys114Asn
ENST00000413592.5:c.84+126A>C ENSP00000391140.1:n.84+126A>C
ENST00000486135.1:c.57A>C ENSP00000441569.1:p.Lys19Asn
ENST00000494660.6:c.57A>C ENSP00000437361.1:p.Lys19Asn
NM_032601.3:c.342A>C NP_115990.3:p.Lys114Asn
XM_005264613.2:c.216+126A>C XP_005264670.1:n.216+126A>C
XR_939729.1:n.411A>C
XR_939729.2:n.411A>C
NM_032601.4:c.342A>C MANE Select NP_115990.3:p.Lys114Asn