Canonical Allele Identifier: CA895917587

Gene: TMEM131

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.97990307T>A , CM000664.2:g.97990307T>A	GRCh38
NC_000002.11:g.98606770T>A , CM000664.1:g.98606770T>A	GRCh37
NC_000002.10:g.97973202T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_015348.2:c.187+5169A>T MANE Select	NP_056163.1:n.187+5169A>T
ENST00000186436.10:c.187+5169A>T MANE Select	ENSP00000186436.5:n.187+5169A>T
NM_015348.1:c.187+5169A>T	NP_056163.1:n.187+5169A>T
ENST00000186436.9:c.187+5169A>T	ENSP00000186436.5:n.187+5169A>T
ENST00000418629.6:c.69+5169A>T
ENST00000489507.1:n.76+5169A>T
XM_005263909.1:c.187+5169A>T	XP_005263966.1:n.187+5169A>T
XM_005263910.1:c.187+5169A>T	XP_005263967.1:n.187+5169A>T
XM_005263911.1:c.187+5169A>T	XP_005263968.1:n.187+5169A>T
XM_005263912.2:c.187+5169A>T	XP_005263969.1:n.187+5169A>T
XM_005263912.3:c.187+5169A>T	XP_005263969.1:n.187+5169A>T
XM_011510869.1:c.187+5169A>T	XP_011509171.1:n.187+5169A>T
XR_001738682.1:n.451+5169A>T