Canonical Allele Identifier: CA358345013

Gene: MMAA

Linked Data

• MyVariant Identifiers: chr4:g.146576339A>C (hg19) ; chr4:g.145655187A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.145655187A>C , CM000666.2:g.145655187A>C	GRCh38
NC_000004.11:g.146576339A>C , CM000666.1:g.146576339A>C	GRCh37
NC_000004.10:g.146795789A>C	NCBI36
NG_007536.1:g.40890A>C
NG_007536.2:g.61146A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541599.5:c.1010A>C	ENSP00000442284.3:p.Glu337Ala
ENST00000647947.1:c.*794A>C	ENSP00000496781.1:n.*794A>C
ENST00000648388.1:c.1010A>C	ENSP00000497046.1:p.Glu337Ala
ENST00000649156.2:c.1010A>C MANE Select	ENSP00000497008.1:p.Glu337Ala
ENST00000649173.1:c.944A>C	ENSP00000497871.1:p.Glu315Ala
ENST00000649704.1:c.1010A>C	ENSP00000497680.1:p.Glu337Ala
ENST00000679563.1:c.1010A>C	ENSP00000506503.1:p.Glu337Ala
ENST00000679930.1:c.*529A>C	ENSP00000506293.1:n.*529A>C
ENST00000281317.9:c.1010A>C	ENSP00000281317.5:p.Glu337Ala
ENST00000503730.1:n.420A>C
ENST00000511969.4:c.*141A>C	ENSP00000427422.1:n.*141A>C
ENST00000541599.4:c.1010A>C	ENSP00000442284.2:p.Glu337Ala
NM_172250.2:c.1010A>C	NP_758454.1:p.Glu337Ala
XM_011531684.1:c.1010A>C	XP_011529986.1:p.Glu337Ala
XM_011531685.1:c.1010A>C	XP_011529987.1:p.Glu337Ala
XM_011531686.1:c.515A>C	XP_011529988.1:p.Glu172Ala
NM_172250.3:c.1010A>C MANE Select	NP_758454.1:p.Glu337Ala
XM_011531684.3:c.1010A>C	XP_011529986.1:p.Glu337Ala
XM_011531685.2:c.1010A>C	XP_011529987.1:p.Glu337Ala
XM_011531686.2:c.515A>C	XP_011529988.1:p.Glu172Ala
NM_001375644.1:c.1010A>C	NP_001362573.1:p.Glu337Ala