Canonical Allele Identifier: CA6359897

Gene: TMEM45B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.129852625T>C , CM000673.2:g.129852625T>C	GRCh38
NC_000011.9:g.129722520T>C , CM000673.1:g.129722520T>C	GRCh37
NC_000011.8:g.129227730T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281441.8:c.143T>C MANE Select	ENSP00000281441.3:p.Val48Ala
ENST00000281441.7:c.143T>C	ENSP00000281441.3:p.Val48Ala
ENST00000524567.1:c.143T>C	ENSP00000436293.1:p.Val48Ala
ENST00000527754.1:n.294T>C
ENST00000529381.1:n.179T>C
NM_138788.3:c.143T>C	NP_620143.1:p.Val48Ala
XM_005271400.3:c.143T>C	XP_005271457.1:p.Val48Ala
XM_011542586.1:c.143T>C	XP_011540888.1:p.Val48Ala
XM_011542587.1:c.143T>C	XP_011540889.1:p.Val48Ala
XM_011542588.1:c.143T>C	XP_011540890.1:p.Val48Ala
NM_001331210.1:c.143T>C	NP_001318139.1:p.Val48Ala
NM_001331211.1:c.143T>C	NP_001318140.1:p.Val48Ala
NM_001331212.1:c.143T>C	NP_001318141.1:p.Val48Ala
NM_138788.4:c.143T>C	NP_620143.1:p.Val48Ala
XM_017017188.1:c.143T>C	XP_016872677.1:p.Val48Ala
XM_017017189.1:c.143T>C	XP_016872678.1:p.Val48Ala
NM_138788.5:c.143T>C MANE Select	NP_620143.1:p.Val48Ala
NM_001331210.2:c.143T>C	NP_001318139.1:p.Val48Ala
NM_001331211.2:c.143T>C	NP_001318140.1:p.Val48Ala
NM_001331212.2:c.143T>C	NP_001318141.1:p.Val48Ala