Canonical Allele Identifier: CA38716145

Gene: ARF1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.228097217T>C , CM000663.2:g.228097217T>C	GRCh38
NC_000001.10:g.228284918T>C , CM000663.1:g.228284918T>C	GRCh37
NC_000001.9:g.226351541T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001658.4:c.103T>C MANE Select	NP_001649.1:p.Tyr35His
ENST00000272102.10:c.103T>C MANE Select	ENSP00000272102.5:p.Tyr35His
NM_001024226.1:c.103T>C	NP_001019397.1:p.Tyr35His
NM_001024226.2:c.103T>C	NP_001019397.1:p.Tyr35His
NM_001024227.1:c.103T>C	NP_001019398.1:p.Tyr35His
NM_001024228.1:c.103T>C	NP_001019399.1:p.Tyr35His
NM_001024228.2:c.103T>C	NP_001019399.1:p.Tyr35His
NM_001658.3:c.103T>C	NP_001649.1:p.Tyr35His
ENST00000272102.9:c.103T>C	ENSP00000272102.5:p.Tyr35His
ENST00000469235.5:n.300T>C
ENST00000470558.5:n.202T>C
ENST00000470670.5:n.176T>C
ENST00000473949.5:n.254T>C
ENST00000477451.5:n.568T>C
ENST00000478336.5:n.378T>C
ENST00000478424.5:n.250T>C
ENST00000482962.5:n.271T>C
ENST00000490705.1:n.724T>C
ENST00000490705.2:c.103T>C	ENSP00000514662.1:p.Tyr35His
ENST00000497165.5:n.302T>C
ENST00000540651.5:c.103T>C	ENSP00000442980.1:p.Tyr35His
ENST00000541182.1:c.103T>C	ENSP00000440005.1:p.Tyr35His
XM_017001233.1:c.103T>C	XP_016856722.1:p.Tyr35His