Canonical Allele Identifier: CA2667114982

Gene: TMEM39A

Linked Data

• gnomAD v4: 3-119431918-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119431918A>G , CM000665.2:g.119431918A>G	GRCh38
NC_000003.11:g.119150765A>G , CM000665.1:g.119150765A>G	GRCh37
NC_000003.10:g.120633455A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000319172.10:c.*63T>C MANE Select	ENSP00000326063.5:n.*63T>C
ENST00000319172.9:c.*63T>C	ENSP00000326063.5:n.*63T>C
ENST00000438581.6:c.*1198T>C	ENSP00000402149.2:n.*1198T>C
ENST00000473684.5:c.625T>C	ENSP00000420432.1:n.625T>C
NM_018266.2:c.*63T>C	NP_060736.1:n.*63T>C
NR_073506.1:n.2060T>C
XM_005247578.1:c.*275T>C	XP_005247635.1:n.*275T>C
XM_006713687.1:c.*63T>C	XP_006713750.1:n.*63T>C
XM_005247578.2:c.*275T>C	XP_005247635.1:n.*275T>C
XM_006713687.2:c.*63T>C	XP_006713750.1:n.*63T>C
XM_017006788.2:c.*63T>C	XP_016862277.1:n.*63T>C
XR_001740197.2:n.2082T>C
XR_001740198.2:n.1998T>C
NM_018266.3:c.*63T>C MANE Select	NP_060736.1:n.*63T>C
NR_073506.2:n.1993T>C