Canonical Allele Identifier: CA2658010868

Gene: MATN3

Linked Data

• gnomAD v4: 2-20005659-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.20005659_20005660insG , CM000664.2:g.20005659_20005660insG	GRCh38
NC_000002.11:g.20205420_20205421insG , CM000664.1:g.20205420_20205421insG	GRCh37
NC_000002.10:g.20068901_20068902insG	NCBI36
NG_008087.1:g.12035_12036insC

Transcript Alleles

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