Canonical Allele Identifier: CA395618796

Gene: CTF1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30902244T>C , CM000678.2:g.30902244T>C	GRCh38
NC_000016.9:g.30913565T>C , CM000678.1:g.30913565T>C	GRCh37
NC_000016.8:g.30821066T>C	NCBI36
NG_009171.1:g.10638T>C , LRG_408:g.10638T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279804.3:c.311T>C MANE Select	ENSP00000279804.2:p.Val104Ala
ENST00000279804.2:c.311T>C	ENSP00000279804.2:p.Val104Ala
ENST00000395019.3:c.308T>C	ENSP00000378465.3:p.Val103Ala
NM_001142544.1:c.308T>C	NP_001136016.1:p.Val103Ala
NM_001330.3:c.311T>C , LRG_408t1:c.311T>C	NP_001321.1:p.Val104Ala
XM_011545759.1:c.377T>C	XP_011544061.1:p.Val126Ala
XM_011545760.1:c.335T>C	XP_011544062.1:p.Val112Ala
XM_011545759.2:c.377T>C	XP_011544061.1:p.Val126Ala
XM_011545760.2:c.335T>C	XP_011544062.1:p.Val112Ala
NM_001142544.2:c.308T>C	NP_001136016.1:p.Val103Ala
NM_001142544.3:c.308T>C	NP_001136016.1:p.Val103Ala
NM_001330.5:c.311T>C MANE Select	NP_001321.1:p.Val104Ala
NR_165660.1:n.449T>C