Canonical Allele Identifier: CA481712472

Gene: MMAB

Linked Data

• MyVariant Identifiers: chr12:g.110006604T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109568799T>A , CM000674.2:g.109568799T>A	GRCh38
NC_000012.11:g.110006604T>A , CM000674.1:g.110006604T>A	GRCh37
NC_000012.10:g.108490987T>A	NCBI36
NG_007096.1:g.9699A>T
NG_007702.1:g.105T>A , LRG_156:g.105T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545712.7:c.261A>T MANE Select	ENSP00000445920.1:p.Gly87=
ENST00000420167.6:c.*90A>T	ENSP00000416136.2:n.*90A>T
ENST00000503497.7:c.261A>T	ENSP00000474881.1:p.Gly87=
ENST00000536760.1:n.264A>T
ENST00000537236.2:c.261A>T	ENSP00000483818.1:p.Gly87=
ENST00000537496.5:c.261A>T	ENSP00000444793.1:p.Gly87=
ENST00000540016.5:c.135-3623A>T	ENSP00000474582.1:n.135-3623A>T
ENST00000541763.6:c.261A>T	ENSP00000474981.1:p.Gly87=
ENST00000542390.5:n.288A>T
ENST00000544051.5:c.*55A>T	ENSP00000438079.1:n.*55A>T
ENST00000545712.6:c.261A>T	ENSP00000445920.1:p.Gly87=
NM_052845.3:c.261A>T	NP_443077.1:p.Gly87=
NR_038118.1:n.334A>T
XM_024448961.1:c.261A>T	XP_024304729.1:p.Gly87=
NM_052845.4:c.261A>T MANE Select	NP_443077.1:p.Gly87=
NR_038118.2:n.285A>T