Canonical Allele Identifier: CA2838383758

Gene: TMEM181

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158559920A>G , CM000668.2:g.158559920A>G	GRCh38
NC_000006.11:g.158980952A>G , CM000668.1:g.158980952A>G	GRCh37
NC_000006.10:g.158900940A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367090.4:c.132-13500A>G	ENSP00000356057.4:n.132-13500A>G
ENST00000367090.3:c.420-13500A>G	ENSP00000356057.3:n.420-13500A>G
NM_020823.1:c.420-13500A>G	NP_065874.1:n.420-13500A>G
XM_011535999.1:c.420-13500A>G	XP_011534301.1:n.420-13500A>G
XM_011536000.1:c.420-13500A>G	XP_011534302.1:n.420-13500A>G
XM_011536003.1:c.420-13500A>G	XP_011534305.1:n.420-13500A>G
XM_011536003.2:c.420-13500A>G	XP_011534305.1:n.420-13500A>G
NM_001376817.1:c.132-13500A>G	NP_001363746.1:n.132-13500A>G
NM_001376855.1:c.17-21020A>G	NP_001363784.1:n.17-21020A>G
NM_001376856.1:c.16+23055A>G	NP_001363785.1:n.16+23055A>G
NM_020823.2:c.132-13500A>G	NP_065874.2:n.132-13500A>G