Canonical Allele Identifier: CA2699456872

Gene: MCEE

Linked Data

• dbSNP Id: rs2103640132

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71124607T>G , CM000664.2:g.71124607T>G	GRCh38
NC_000002.11:g.71351737T>G , CM000664.1:g.71351737T>G	GRCh37
NC_000002.10:g.71205245T>G	NCBI36
NG_008977.1:g.10658A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244217.6:c.41-64A>C MANE Select	ENSP00000244217.5:n.41-64A>C
ENST00000244217.5:c.41-64A>C	ENSP00000244217.5:n.41-64A>C
ENST00000486135.1:c.-245-64A>C	ENSP00000441569.1:n.-245-64A>C
ENST00000494660.6:c.-245-64A>C	ENSP00000437361.1:n.-245-64A>C
NM_032601.3:c.41-64A>C	NP_115990.3:n.41-64A>C
XM_005264613.2:c.41-64A>C	XP_005264670.1:n.41-64A>C
XR_939729.1:n.110-64A>C
XR_939729.2:n.110-64A>C
NM_032601.4:c.41-64A>C MANE Select	NP_115990.3:n.41-64A>C