Canonical Allele Identifier: CA398288523

Gene: TRIM16

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.15642767T>A , CM000679.2:g.15642767T>A	GRCh38
NC_000017.10:g.15546081T>A , CM000679.1:g.15546081T>A	GRCh37
NC_000017.9:g.15486806T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649191.2:c.569A>T MANE Select	ENSP00000497185.2:p.Asn190Ile
ENST00000336708.11:c.569A>T	ENSP00000338989.7:p.Asn190Ile
ENST00000416464.6:c.179A>T	ENSP00000399918.2:p.Asn60Ile
ENST00000455584.2:c.569A>T	ENSP00000402644.2:p.Asn190Ile
ENST00000460728.5:n.699A>T
ENST00000473540.5:n.437A>T
ENST00000577372.5:c.-80A>T	ENSP00000463293.1:n.-80A>T
ENST00000577886.5:c.-80A>T	ENSP00000462903.1:n.-80A>T
ENST00000578237.5:c.569A>T	ENSP00000463188.1:p.Asn190Ile
ENST00000578744.5:c.191A>T	ENSP00000465907.1:p.Asn64Ile
ENST00000579219.5:c.-80A>T	ENSP00000463639.1:n.-80A>T
ENST00000579272.5:n.535A>T
ENST00000580110.5:c.-80A>T	ENSP00000464072.1:n.-80A>T
ENST00000581200.1:c.179A>T	ENSP00000463360.1:p.Asn60Ile
ENST00000581224.5:n.703A>T
NM_006470.3:c.569A>T	NP_006461.3:p.Asn190Ile
NM_001348119.1:c.569A>T MANE Select	NP_001335048.1:p.Asn190Ile
NM_001348120.1:c.569A>T	NP_001335049.1:p.Asn190Ile
NM_001348121.1:c.179A>T	NP_001335050.1:p.Asn60Ile
NM_001348122.1:c.179A>T	NP_001335051.1:p.Asn60Ile
NM_001348124.1:c.-80A>T	NP_001335053.1:n.-80A>T
NM_001348125.1:c.-80A>T	NP_001335054.1:n.-80A>T
NM_001348126.1:c.83A>T	NP_001335055.1:p.Asn28Ile
NM_006470.4:c.569A>T	NP_006461.3:p.Asn190Ile