Canonical Allele Identifier: CA1259891378

Gene: MCEE

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71124570_71124573delinsCCTT , CM000664.2:g.71124570_71124573delinsCCTT	GRCh38
NC_000002.11:g.71351700_71351703delinsCCTT , CM000664.1:g.71351700_71351703delinsCCTT	GRCh37
NC_000002.10:g.71205208_71205211delinsCCTT	NCBI36
NG_008977.1:g.10692_10695delinsAAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244217.6:c.41-30_41-27delinsAAGG MANE Select	ENSP00000244217.5:n.41-30_41-27delinsAAGG
ENST00000244217.5:c.41-30_41-27delinsAAGG	ENSP00000244217.5:n.41-30_41-27delinsAAGG
ENST00000486135.1:c.-245-30_-245-27delinsAAGG	ENSP00000441569.1:n.-245-30_-245-27delinsAAGG
ENST00000494660.6:c.-245-30_-245-27delinsAAGG	ENSP00000437361.1:n.-245-30_-245-27delinsAAGG
NM_032601.3:c.41-30_41-27delinsAAGG	NP_115990.3:n.41-30_41-27delinsAAGG
XM_005264613.2:c.41-30_41-27delinsAAGG	XP_005264670.1:n.41-30_41-27delinsAAGG
XR_939729.1:n.110-30_110-27delinsAAGG
XR_939729.2:n.110-30_110-27delinsAAGG
NM_032601.4:c.41-30_41-27delinsAAGG MANE Select	NP_115990.3:n.41-30_41-27delinsAAGG