Canonical Allele Identifier: CA2620810013

Gene: MMAB

Linked Data

• gnomAD v4: 12-109556966-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109556966A>T , CM000674.2:g.109556966A>T	GRCh38
NC_000012.11:g.109994771A>T , CM000674.1:g.109994771A>T	GRCh37
NC_000012.10:g.108479154A>T	NCBI36
NG_007096.1:g.21532T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545712.7:c.*62T>A MANE Select	ENSP00000445920.1:n.*62T>A
ENST00000537496.5:c.*380T>A	ENSP00000444793.1:n.*380T>A
ENST00000540016.5:c.*62T>A	ENSP00000474582.1:n.*62T>A
ENST00000541763.6:c.1040T>A	ENSP00000474981.1:n.1040T>A
ENST00000544051.5:c.*696T>A	ENSP00000438079.1:n.*696T>A
ENST00000545712.6:c.*62T>A	ENSP00000445920.1:n.*62T>A
NM_052845.3:c.*62T>A	NP_443077.1:n.*62T>A
NR_038118.1:n.975T>A
XM_011538266.1:c.*162T>A	XP_011536568.1:n.*162T>A
XM_011538267.1:c.*162T>A	XP_011536569.1:n.*162T>A
XM_011538268.1:c.*62T>A	XP_011536570.1:n.*62T>A
XM_011538269.1:c.*62T>A	XP_011536571.1:n.*62T>A
XM_011538267.3:c.*162T>A	XP_011536569.1:n.*162T>A
XM_011538268.2:c.*62T>A	XP_011536570.1:n.*62T>A
XM_011538269.2:c.*62T>A	XP_011536571.1:n.*62T>A
NM_052845.4:c.*62T>A MANE Select	NP_443077.1:n.*62T>A
NR_038118.2:n.926T>A