Canonical Allele Identifier: CA1882633818

Gene: SURF1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133352339_133352349delinsCACATGTGAGA , CM000671.2:g.133352339_133352349delinsCACATGTGAGA	GRCh38
NC_000009.10:g.135209015_135209025delinsCACATGTGAGA	NCBI36
NG_008477.1:g.9158_9168delinsTCTCACATGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371974.8:c.751+97_751+107delinsTCTCACATGTG MANE Select	ENSP00000361042.3:n.751+97_751+107delinsTCTCACATGTG
ENST00000371974.7:c.751+97_751+107delinsTCTCACATGTG	ENSP00000361042.3:n.751+97_751+107delinsTCTCACATGTG
ENST00000437995.1:n.661+97_661+107delinsTCTCACATGTG
ENST00000495952.5:n.741+97_741+107delinsTCTCACATGTG
ENST00000615505.4:c.424+97_424+107delinsTCTCACATGTG	ENSP00000482067.1:n.424+97_424+107delinsTCTCACATGTG
NM_001280787.1:c.424+97_424+107delinsTCTCACATGTG	NP_001267716.1:n.424+97_424+107delinsTCTCACATGTG
NM_003172.3:c.751+97_751+107delinsTCTCACATGTG	NP_003163.1:n.751+97_751+107delinsTCTCACATGTG
XM_011518942.1:c.424+97_424+107delinsTCTCACATGTG	XP_011517244.1:n.424+97_424+107delinsTCTCACATGTG
NM_003172.4:c.751+97_751+107delinsTCTCACATGTG MANE Select	NP_003163.1:n.751+97_751+107delinsTCTCACATGTG