Canonical Allele Identifier: CA386635535

Gene: MMAB

Linked Data

• MyVariant Identifiers: chr12:g.109994877T>G (hg19) ; chr12:g.109557072T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109557072T>G , CM000674.2:g.109557072T>G	GRCh38
NC_000012.11:g.109994877T>G , CM000674.1:g.109994877T>G	GRCh37
NC_000012.10:g.108479260T>G	NCBI36
NG_007096.1:g.21426A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545712.7:c.709A>C MANE Select	ENSP00000445920.1:p.Ile237Leu
ENST00000537496.5:c.*274A>C	ENSP00000444793.1:n.*274A>C
ENST00000540016.5:c.553A>C	ENSP00000474582.1:p.Ile185Leu
ENST00000541763.6:c.934A>C	ENSP00000474981.1:n.934A>C
ENST00000544051.5:c.*590A>C	ENSP00000438079.1:n.*590A>C
ENST00000545712.6:c.709A>C	ENSP00000445920.1:p.Ile237Leu
NM_052845.3:c.709A>C	NP_443077.1:p.Ile237Leu
NR_038118.1:n.869A>C
XM_011538266.1:c.*56A>C	XP_011536568.1:n.*56A>C
XM_011538267.1:c.*56A>C	XP_011536569.1:n.*56A>C
XM_011538268.1:c.436A>C	XP_011536570.1:p.Ile146Leu
XM_011538269.1:c.433A>C	XP_011536571.1:p.Ile145Leu
XM_011538267.3:c.*56A>C	XP_011536569.1:n.*56A>C
XM_011538268.2:c.436A>C	XP_011536570.1:p.Ile146Leu
XM_011538269.2:c.433A>C	XP_011536571.1:p.Ile145Leu
NM_052845.4:c.709A>C MANE Select	NP_443077.1:p.Ile237Leu
NR_038118.2:n.820A>C