Canonical Allele Identifier: CA2925599

Gene: TMEM165

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55424556G>A , CM000666.2:g.55424556G>A	GRCh38
NC_000004.11:g.56290723G>A , CM000666.1:g.56290723G>A	GRCh37
NC_000004.10:g.55985480G>A	NCBI36
NG_032881.1:g.33644G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_018475.5:c.811G>A MANE Select	NP_060945.2:p.Val271Met
ENST00000381334.10:c.811G>A MANE Select	ENSP00000370736.5:p.Val271Met
NM_018475.4:c.811G>A	NP_060945.2:p.Val271Met
NR_073070.1:n.1191G>A
NR_073070.2:n.1147G>A
ENST00000381334.9:c.811G>A	ENSP00000370736.5:p.Val271Met
ENST00000506103.2:c.265G>A
ENST00000506198.5:c.226G>A	ENSP00000425449.1:p.Val76Met
ENST00000508404.5:c.*683G>A	ENSP00000422639.1:n.*683G>A
ENST00000508561.5:n.507G>A
ENST00000509575.1:n.314G>A
ENST00000514904.5:n.1265G>A
ENST00000515591.1:n.1443G>A
ENST00000608091.1:c.321G>A
XM_011534394.1:c.811G>A	XP_011532696.1:p.Val271Met
XM_011534394.3:c.811G>A	XP_011532696.1:p.Val271Met
XM_017008412.1:c.622G>A	XP_016863901.1:p.Val208Met
XR_001741287.2:n.1527G>A