Canonical Allele Identifier: CA386637414

Gene: MMAB

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109561472C>T , CM000674.2:g.109561472C>T	GRCh38
NC_000012.11:g.109999277C>T , CM000674.1:g.109999277C>T	GRCh37
NC_000012.10:g.108483660C>T	NCBI36
NG_007096.1:g.17026G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_052845.4:c.467G>A MANE Select	NP_443077.1:p.Trp156Ter
ENST00000545712.7:c.467G>A MANE Select	ENSP00000445920.1:p.Trp156Ter
NM_052845.3:c.467G>A	NP_443077.1:p.Trp156Ter
NR_038118.1:n.540G>A
NR_038118.2:n.491G>A
ENST00000537496.5:c.467G>A	ENSP00000444793.1:p.Trp156Ter
ENST00000540016.5:c.311G>A	ENSP00000474582.1:p.Trp104Ter
ENST00000541763.6:c.467G>A	ENSP00000474981.1:p.Trp156Ter
ENST00000544051.5:c.*261G>A	ENSP00000438079.1:n.*261G>A
ENST00000545712.6:c.467G>A	ENSP00000445920.1:p.Trp156Ter
XM_011538266.1:c.225G>A	XP_011536568.1:p.Val75=
XM_011538267.1:c.225G>A	XP_011536569.1:p.Val75=
XM_011538267.3:c.225G>A	XP_011536569.1:p.Val75=
XM_011538268.1:c.194G>A	XP_011536570.1:p.Trp65Ter
XM_011538268.2:c.194G>A	XP_011536570.1:p.Trp65Ter
XM_011538269.1:c.191G>A	XP_011536571.1:p.Trp64Ter
XM_011538269.2:c.191G>A	XP_011536571.1:p.Trp64Ter
XM_024448961.1:c.467G>A	XP_024304729.1:p.Trp156Ter