Canonical Allele Identifier: CA441478359

Gene: MMAA

Linked Data

• MyVariant Identifiers: chr4:g.146567239A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.145646087A>C , CM000666.2:g.145646087A>C	GRCh38
NC_000004.11:g.146567239A>C , CM000666.1:g.146567239A>C	GRCh37
NC_000004.10:g.146786689A>C	NCBI36
NG_007536.1:g.31790A>C
NG_007536.2:g.52046A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541599.5:c.664A>C	ENSP00000442284.3:p.Arg222=
ENST00000647947.1:c.*448A>C	ENSP00000496781.1:n.*448A>C
ENST00000648388.1:c.664A>C	ENSP00000497046.1:p.Arg222=
ENST00000649156.2:c.664A>C MANE Select	ENSP00000497008.1:p.Arg222=
ENST00000649173.1:c.664A>C	ENSP00000497871.1:p.Arg222=
ENST00000649704.1:c.664A>C	ENSP00000497680.1:p.Arg222=
ENST00000679563.1:c.664A>C	ENSP00000506503.1:p.Arg222=
ENST00000679930.1:c.*183A>C	ENSP00000506293.1:n.*183A>C
ENST00000281317.9:c.664A>C	ENSP00000281317.5:p.Arg222=
ENST00000506919.1:n.1152A>C
ENST00000511969.4:c.664A>C	ENSP00000427422.1:p.Arg222=
ENST00000541599.4:c.664A>C	ENSP00000442284.2:p.Arg222=
NM_172250.2:c.664A>C	NP_758454.1:p.Arg222=
XM_011531684.1:c.664A>C	XP_011529986.1:p.Arg222=
XM_011531685.1:c.664A>C	XP_011529987.1:p.Arg222=
XM_011531686.1:c.169A>C	XP_011529988.1:p.Arg57=
NM_172250.3:c.664A>C MANE Select	NP_758454.1:p.Arg222=
XM_011531684.3:c.664A>C	XP_011529986.1:p.Arg222=
XM_011531685.2:c.664A>C	XP_011529987.1:p.Arg222=
XM_011531686.2:c.169A>C	XP_011529988.1:p.Arg57=
NM_001375644.1:c.664A>C	NP_001362573.1:p.Arg222=