Canonical Allele Identifier: CA358344806

Gene: MMAA

Linked Data

• MyVariant Identifiers: chr4:g.146576315C>A (hg19) ; chr4:g.145655163C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.145655163C>A , CM000666.2:g.145655163C>A	GRCh38
NC_000004.11:g.146576315C>A , CM000666.1:g.146576315C>A	GRCh37
NC_000004.10:g.146795765C>A	NCBI36
NG_007536.1:g.40866C>A
NG_007536.2:g.61122C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000541599.5:c.986C>A	ENSP00000442284.3:p.Ala329Asp
ENST00000647947.1:c.*770C>A	ENSP00000496781.1:n.*770C>A
ENST00000648388.1:c.986C>A	ENSP00000497046.1:p.Ala329Asp
ENST00000649156.2:c.986C>A MANE Select	ENSP00000497008.1:p.Ala329Asp
ENST00000649173.1:c.920C>A	ENSP00000497871.1:p.Ala307Asp
ENST00000649704.1:c.986C>A	ENSP00000497680.1:p.Ala329Asp
ENST00000679563.1:c.986C>A	ENSP00000506503.1:p.Ala329Asp
ENST00000679930.1:c.*505C>A	ENSP00000506293.1:n.*505C>A
ENST00000281317.9:c.986C>A	ENSP00000281317.5:p.Ala329Asp
ENST00000503730.1:n.396C>A
ENST00000511969.4:c.*117C>A	ENSP00000427422.1:n.*117C>A
ENST00000541599.4:c.986C>A	ENSP00000442284.2:p.Ala329Asp
NM_172250.2:c.986C>A	NP_758454.1:p.Ala329Asp
XM_011531684.1:c.986C>A	XP_011529986.1:p.Ala329Asp
XM_011531685.1:c.986C>A	XP_011529987.1:p.Ala329Asp
XM_011531686.1:c.491C>A	XP_011529988.1:p.Ala164Asp
NM_172250.3:c.986C>A MANE Select	NP_758454.1:p.Ala329Asp
XM_011531684.3:c.986C>A	XP_011529986.1:p.Ala329Asp
XM_011531685.2:c.986C>A	XP_011529987.1:p.Ala329Asp
XM_011531686.2:c.491C>A	XP_011529988.1:p.Ala164Asp
NM_001375644.1:c.986C>A	NP_001362573.1:p.Ala329Asp