Canonical Allele Identifier: CA1501207365

Gene: MMAA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.145655265A= , CM000666.2:g.145655265A=	GRCh38
NC_000004.11:g.146576417A= , CM000666.1:g.146576417A=	GRCh37
NC_000004.10:g.146795867A=	NCBI36
NG_007536.1:g.40968A=
NG_007536.2:g.61224A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541599.5:c.1088A=	ENSP00000442284.3:p.Gln363=
ENST00000647947.1:c.*872A=	ENSP00000496781.1:n.*872A=
ENST00000648388.1:c.1088A=	ENSP00000497046.1:p.Gln363=
ENST00000649156.2:c.1088A= MANE Select	ENSP00000497008.1:p.Gln363=
ENST00000649173.1:c.1022A=	ENSP00000497871.1:p.Gln341=
ENST00000649704.1:c.1088A=	ENSP00000497680.1:p.Gln363=
ENST00000679563.1:c.1088A=	ENSP00000506503.1:p.Gln363=
ENST00000679930.1:c.*607A=	ENSP00000506293.1:n.*607A=
ENST00000281317.9:c.1088A=	ENSP00000281317.5:p.Gln363=
ENST00000503730.1:n.498A=
ENST00000511969.4:c.*219A=	ENSP00000427422.1:n.*219A=
ENST00000541599.4:c.1088A=	ENSP00000442284.2:p.Gln363=
NM_172250.2:c.1088A=	NP_758454.1:p.Gln363=
XM_011531684.1:c.1088A=	XP_011529986.1:p.Gln363=
XM_011531685.1:c.1088A=	XP_011529987.1:p.Gln363=
XM_011531686.1:c.593A=	XP_011529988.1:p.Gln198=
NM_172250.3:c.1088A= MANE Select	NP_758454.1:p.Gln363=
XM_011531684.3:c.1088A=	XP_011529986.1:p.Gln363=
XM_011531685.2:c.1088A=	XP_011529987.1:p.Gln363=
XM_011531686.2:c.593A=	XP_011529988.1:p.Gln198=
NM_001375644.1:c.1088A=	NP_001362573.1:p.Gln363=