Canonical Allele Identifier: CA386635652

Gene: MMAB

Linked Data

• MyVariant Identifiers: chr12:g.109994907C>A (hg19) ; chr12:g.109557102C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109557102C>A , CM000674.2:g.109557102C>A	GRCh38
NC_000012.11:g.109994907C>A , CM000674.1:g.109994907C>A	GRCh37
NC_000012.10:g.108479290C>A	NCBI36
NG_007096.1:g.21396G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545712.7:c.679G>T MANE Select	ENSP00000445920.1:p.Ala227Ser
ENST00000537496.5:c.*244G>T	ENSP00000444793.1:n.*244G>T
ENST00000540016.5:c.523G>T	ENSP00000474582.1:p.Ala175Ser
ENST00000541763.6:c.904G>T	ENSP00000474981.1:n.904G>T
ENST00000544051.5:c.*560G>T	ENSP00000438079.1:n.*560G>T
ENST00000545712.6:c.679G>T	ENSP00000445920.1:p.Ala227Ser
NM_052845.3:c.679G>T	NP_443077.1:p.Ala227Ser
NR_038118.1:n.839G>T
XM_011538266.1:c.*26G>T	XP_011536568.1:n.*26G>T
XM_011538267.1:c.*26G>T	XP_011536569.1:n.*26G>T
XM_011538268.1:c.406G>T	XP_011536570.1:p.Ala136Ser
XM_011538269.1:c.403G>T	XP_011536571.1:p.Ala135Ser
XM_011538267.3:c.*26G>T	XP_011536569.1:n.*26G>T
XM_011538268.2:c.406G>T	XP_011536570.1:p.Ala136Ser
XM_011538269.2:c.403G>T	XP_011536571.1:p.Ala135Ser
NM_052845.4:c.679G>T MANE Select	NP_443077.1:p.Ala227Ser
NR_038118.2:n.790G>T