Canonical Allele Identifier: CA2659522982

Gene: MCEE

Linked Data

• gnomAD v4: 2-71124622-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71124622A>G , CM000664.2:g.71124622A>G	GRCh38
NC_000002.11:g.71351752A>G , CM000664.1:g.71351752A>G	GRCh37
NC_000002.10:g.71205260A>G	NCBI36
NG_008977.1:g.10643T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244217.6:c.41-79T>C MANE Select	ENSP00000244217.5:n.41-79T>C
ENST00000244217.5:c.41-79T>C	ENSP00000244217.5:n.41-79T>C
ENST00000486135.1:c.-245-79T>C	ENSP00000441569.1:n.-245-79T>C
ENST00000494660.6:c.-245-79T>C	ENSP00000437361.1:n.-245-79T>C
NM_032601.3:c.41-79T>C	NP_115990.3:n.41-79T>C
XM_005264613.2:c.41-79T>C	XP_005264670.1:n.41-79T>C
XR_939729.1:n.110-79T>C
XR_939729.2:n.110-79T>C
NM_032601.4:c.41-79T>C MANE Select	NP_115990.3:n.41-79T>C