Canonical Allele Identifier: CA11629324

Gene: MME

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.155083576T>C , CM000665.2:g.155083576T>C	GRCh38
NC_000003.11:g.154801365T>C , CM000665.1:g.154801365T>C	GRCh37
NC_000003.10:g.156284059T>C	NCBI36
NG_051105.1:g.64453T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360490.7:c.-10-582T>C MANE Select	ENSP00000353679.2:n.-10-582T>C
ENST00000460393.6:c.-10-582T>C	ENSP00000418525.1:n.-10-582T>C
ENST00000473730.6:c.-10-582T>C	ENSP00000420542.2:n.-10-582T>C
ENST00000491026.6:c.-10-582T>C	ENSP00000418791.2:n.-10-582T>C
ENST00000615825.2:c.-10-582T>C	ENSP00000478173.2:n.-10-582T>C
ENST00000675418.2:c.-10-582T>C	ENSP00000502021.2:n.-10-582T>C
ENST00000680057.1:c.-227T>C	ENSP00000505211.1:n.-227T>C
ENST00000360490.6:c.-10-582T>C	ENSP00000353679.2:n.-10-582T>C
ENST00000382989.7:c.-10-582T>C	ENSP00000372450.3:n.-10-582T>C
ENST00000460393.5:c.-10-582T>C	ENSP00000418525.1:n.-10-582T>C
ENST00000462745.5:c.-10-582T>C	ENSP00000419653.1:n.-10-582T>C
ENST00000473730.5:c.-10-582T>C	ENSP00000420542.1:n.-10-582T>C
ENST00000481828.5:c.-10-582T>C	ENSP00000420101.1:n.-10-582T>C
ENST00000491026.5:c.-10-582T>C	ENSP00000418791.1:n.-10-582T>C
ENST00000491597.5:n.111-582T>C
ENST00000492661.5:c.-10-582T>C	ENSP00000420389.1:n.-10-582T>C
ENST00000493237.5:c.-10-582T>C	ENSP00000417079.1:n.-10-582T>C
ENST00000497890.1:c.-227T>C	ENSP00000418238.1:n.-227T>C
ENST00000616757.1:c.-10-582T>C	ENSP00000480349.1:n.-10-582T>C
ENST00000625667.2:c.-10-582T>C	ENSP00000485791.1:n.-10-582T>C
NM_000902.3:c.-10-582T>C	NP_000893.2:n.-10-582T>C
NM_007287.2:c.-10-582T>C	NP_009218.2:n.-10-582T>C
NM_007288.2:c.-10-582T>C	NP_009219.2:n.-10-582T>C
NM_007289.2:c.-10-582T>C	NP_009220.2:n.-10-582T>C
XM_006713646.2:c.-10-582T>C	XP_006713709.1:n.-10-582T>C
XM_006713647.2:c.-227T>C	XP_006713710.1:n.-227T>C
XM_011512855.1:c.-10-582T>C	XP_011511157.1:n.-10-582T>C
XM_011512858.1:c.-10-582T>C	XP_011511160.1:n.-10-582T>C
NM_001354642.1:c.-10-582T>C	NP_001341571.1:n.-10-582T>C
NM_001354643.1:c.-10-582T>C	NP_001341572.1:n.-10-582T>C
NM_001354644.1:c.-10-582T>C	NP_001341573.1:n.-10-582T>C
NM_007288.3:c.-10-582T>C	NP_009219.2:n.-10-582T>C
NM_007289.3:c.-10-582T>C	NP_009220.2:n.-10-582T>C
XM_006713647.4:c.-227T>C	XP_006713710.1:n.-227T>C
NM_000902.4:c.-10-582T>C	NP_000893.2:n.-10-582T>C
NM_007287.3:c.-10-582T>C	NP_009218.2:n.-10-582T>C
NM_007289.4:c.-10-582T>C MANE Select	NP_009220.2:n.-10-582T>C
NM_000902.5:c.-10-582T>C	NP_000893.2:n.-10-582T>C
NM_001354642.2:c.-10-582T>C	NP_001341571.1:n.-10-582T>C
NM_007287.4:c.-10-582T>C	NP_009218.2:n.-10-582T>C