Canonical Allele Identifier: CA481710056

Gene: MMAB

Linked Data

• MyVariant Identifiers: chr12:g.109994866T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109557061T>C , CM000674.2:g.109557061T>C	GRCh38
NC_000012.11:g.109994866T>C , CM000674.1:g.109994866T>C	GRCh37
NC_000012.10:g.108479249T>C	NCBI36
NG_007096.1:g.21437A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545712.7:c.720A>G MANE Select	ENSP00000445920.1:p.Lys240=
ENST00000537496.5:c.*285A>G	ENSP00000444793.1:n.*285A>G
ENST00000540016.5:c.564A>G	ENSP00000474582.1:p.Lys188=
ENST00000541763.6:c.945A>G	ENSP00000474981.1:n.945A>G
ENST00000544051.5:c.*601A>G	ENSP00000438079.1:n.*601A>G
ENST00000545712.6:c.720A>G	ENSP00000445920.1:p.Lys240=
NM_052845.3:c.720A>G	NP_443077.1:p.Lys240=
NR_038118.1:n.880A>G
XM_011538266.1:c.*67A>G	XP_011536568.1:n.*67A>G
XM_011538267.1:c.*67A>G	XP_011536569.1:n.*67A>G
XM_011538268.1:c.447A>G	XP_011536570.1:p.Lys149=
XM_011538269.1:c.444A>G	XP_011536571.1:p.Lys148=
XM_011538267.3:c.*67A>G	XP_011536569.1:n.*67A>G
XM_011538268.2:c.447A>G	XP_011536570.1:p.Lys149=
XM_011538269.2:c.444A>G	XP_011536571.1:p.Lys148=
NM_052845.4:c.720A>G MANE Select	NP_443077.1:p.Lys240=
NR_038118.2:n.831A>G