Canonical Allele Identifier: CA386635541

Gene: MMAB

Linked Data

• MyVariant Identifiers: chr12:g.109994880T>A (hg19) ; chr12:g.109557075T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109557075T>A , CM000674.2:g.109557075T>A	GRCh38
NC_000012.11:g.109994880T>A , CM000674.1:g.109994880T>A	GRCh37
NC_000012.10:g.108479263T>A	NCBI36
NG_007096.1:g.21423A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545712.7:c.706A>T MANE Select	ENSP00000445920.1:p.Lys236Ter
ENST00000537496.5:c.*271A>T	ENSP00000444793.1:n.*271A>T
ENST00000540016.5:c.550A>T	ENSP00000474582.1:p.Lys184Ter
ENST00000541763.6:c.931A>T	ENSP00000474981.1:n.931A>T
ENST00000544051.5:c.*587A>T	ENSP00000438079.1:n.*587A>T
ENST00000545712.6:c.706A>T	ENSP00000445920.1:p.Lys236Ter
NM_052845.3:c.706A>T	NP_443077.1:p.Lys236Ter
NR_038118.1:n.866A>T
XM_011538266.1:c.*53A>T	XP_011536568.1:n.*53A>T
XM_011538267.1:c.*53A>T	XP_011536569.1:n.*53A>T
XM_011538268.1:c.433A>T	XP_011536570.1:p.Lys145Ter
XM_011538269.1:c.430A>T	XP_011536571.1:p.Lys144Ter
XM_011538267.3:c.*53A>T	XP_011536569.1:n.*53A>T
XM_011538268.2:c.433A>T	XP_011536570.1:p.Lys145Ter
XM_011538269.2:c.430A>T	XP_011536571.1:p.Lys144Ter
NM_052845.4:c.706A>T MANE Select	NP_443077.1:p.Lys236Ter
NR_038118.2:n.817A>T