Canonical Allele Identifier: CA1346973732

Gene: TMEM43

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14141426G= , CM000665.2:g.14141426G=	GRCh38
NC_000003.11:g.14182926G= , CM000665.1:g.14182926G=	GRCh37
NC_000003.10:g.14157927G=	NCBI36
NG_008975.1:g.21487G= , LRG_435:g.21487G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000432444.2:c.*1031-167G=	ENSP00000395617.1:n.*1031-167G=
ENST00000306077.5:c.1001-167G= MANE Select	ENSP00000303992.5:n.1001-167G=
ENST00000306077.4:c.1001-167G=	ENSP00000303992.4:n.1001-167G=
ENST00000601399.3:n.327+2129G=
ENST00000608606.1:c.236+2129G=
NM_024334.2:c.1001-167G= , LRG_435t1:c.1001-167G=	NP_077310.1:n.1001-167G=
XM_011534109.1:c.896-167G=	XP_011532411.1:n.896-167G=
XM_017007176.2:c.896-167G=	XP_016862665.1:n.896-167G=
NM_024334.3:c.1001-167G= MANE Select	NP_077310.1:n.1001-167G=