Canonical Allele Identifier: CA358345207

Gene: MMAA

Linked Data

• MyVariant Identifiers: chr4:g.146576355G>A (hg19) ; chr4:g.145655203G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.145655203G>A , CM000666.2:g.145655203G>A	GRCh38
NC_000004.11:g.146576355G>A , CM000666.1:g.146576355G>A	GRCh37
NC_000004.10:g.146795805G>A	NCBI36
NG_007536.1:g.40906G>A
NG_007536.2:g.61162G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000541599.5:c.1026G>A	ENSP00000442284.3:p.Met342Ile
ENST00000647947.1:c.*810G>A	ENSP00000496781.1:n.*810G>A
ENST00000648388.1:c.1026G>A	ENSP00000497046.1:p.Met342Ile
ENST00000649156.2:c.1026G>A MANE Select	ENSP00000497008.1:p.Met342Ile
ENST00000649173.1:c.960G>A	ENSP00000497871.1:p.Met320Ile
ENST00000649704.1:c.1026G>A	ENSP00000497680.1:p.Met342Ile
ENST00000679563.1:c.1026G>A	ENSP00000506503.1:p.Met342Ile
ENST00000679930.1:c.*545G>A	ENSP00000506293.1:n.*545G>A
ENST00000281317.9:c.1026G>A	ENSP00000281317.5:p.Met342Ile
ENST00000503730.1:n.436G>A
ENST00000511969.4:c.*157G>A	ENSP00000427422.1:n.*157G>A
ENST00000541599.4:c.1026G>A	ENSP00000442284.2:p.Met342Ile
NM_172250.2:c.1026G>A	NP_758454.1:p.Met342Ile
XM_011531684.1:c.1026G>A	XP_011529986.1:p.Met342Ile
XM_011531685.1:c.1026G>A	XP_011529987.1:p.Met342Ile
XM_011531686.1:c.531G>A	XP_011529988.1:p.Met177Ile
NM_172250.3:c.1026G>A MANE Select	NP_758454.1:p.Met342Ile
XM_011531684.3:c.1026G>A	XP_011529986.1:p.Met342Ile
XM_011531685.2:c.1026G>A	XP_011529987.1:p.Met342Ile
XM_011531686.2:c.531G>A	XP_011529988.1:p.Met177Ile
NM_001375644.1:c.1026G>A	NP_001362573.1:p.Met342Ile