Canonical Allele Identifier: CA43403324

Gene: MATN3

Linked Data

• dbSNP Id: rs141336290

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.20005662_20005663insGAAA , CM000664.2:g.20005662_20005663insGAAA	GRCh38
NC_000002.11:g.20205423_20205424insGAAA , CM000664.1:g.20205423_20205424insGAAA	GRCh37
NC_000002.10:g.20068904_20068905insGAAA	NCBI36
NG_008087.1:g.12035_12036insCTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407540.8:c.790+84_790+85insCTTT MANE Select	ENSP00000383894.3:n.790+84_790+85insCTTT
ENST00000407540.7:c.790+84_790+85insCTTT	ENSP00000383894.3:n.790+84_790+85insCTTT
ENST00000421259.2:c.790+84_790+85insCTTT	ENSP00000398753.2:n.790+84_790+85insCTTT
NM_002381.4:c.790+84_790+85insCTTT	NP_002372.1:n.790+84_790+85insCTTT
NM_002381.5:c.790+84_790+85insCTTT MANE Select	NP_002372.1:n.790+84_790+85insCTTT