Canonical Allele Identifier: CA2620810507

Gene: MMAB

Linked Data

• gnomAD v4: 12-109561130-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109561130G>A , CM000674.2:g.109561130G>A	GRCh38
NC_000012.11:g.109998935G>A , CM000674.1:g.109998935G>A	GRCh37
NC_000012.10:g.108483318G>A	NCBI36
NG_007096.1:g.17368C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545712.7:c.520-26C>T MANE Select	ENSP00000445920.1:n.520-26C>T
ENST00000537496.5:c.*85-26C>T	ENSP00000444793.1:n.*85-26C>T
ENST00000540016.5:c.364-26C>T	ENSP00000474582.1:n.364-26C>T
ENST00000541763.6:c.719C>T	ENSP00000474981.1:n.719C>T
ENST00000544051.5:c.*401-26C>T	ENSP00000438079.1:n.*401-26C>T
ENST00000545712.6:c.520-26C>T	ENSP00000445920.1:n.520-26C>T
NM_052845.3:c.520-26C>T	NP_443077.1:n.520-26C>T
NR_038118.1:n.680-26C>T
XM_011538266.1:c.365-26C>T	XP_011536568.1:n.365-26C>T
XM_011538267.1:c.365-26C>T	XP_011536569.1:n.365-26C>T
XM_011538268.1:c.247-26C>T	XP_011536570.1:n.247-26C>T
XM_011538269.1:c.244-26C>T	XP_011536571.1:n.244-26C>T
XM_011538267.3:c.365-26C>T	XP_011536569.1:n.365-26C>T
XM_011538268.2:c.247-26C>T	XP_011536570.1:n.247-26C>T
XM_011538269.2:c.244-26C>T	XP_011536571.1:n.244-26C>T
XM_024448961.1:c.520-26C>T	XP_024304729.1:n.520-26C>T
NM_052845.4:c.520-26C>T MANE Select	NP_443077.1:n.520-26C>T
NR_038118.2:n.631-26C>T