Canonical Allele Identifier: CA1834541

Gene: TTL

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112501320G>C , CM000664.2:g.112501320G>C	GRCh38
NC_000002.11:g.113258897G>C , CM000664.1:g.113258897G>C	GRCh37
NC_000002.10:g.112975368G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233336.7:c.584G>C MANE Select	ENSP00000233336.5:p.Gly195Ala
ENST00000233336.6:c.584G>C	ENSP00000233336.5:p.Gly195Ala
ENST00000476615.1:n.35G>C
NM_153712.4:c.584G>C	NP_714923.1:p.Gly195Ala
XM_005263599.2:c.584G>C	XP_005263656.1:p.Gly195Ala
XM_011510665.1:c.584G>C	XP_011508967.1:p.Gly195Ala
XM_005263599.3:c.584G>C	XP_005263656.1:p.Gly195Ala
XM_011510665.2:c.584G>C	XP_011508967.1:p.Gly195Ala
NM_153712.5:c.584G>C MANE Select	NP_714923.1:p.Gly195Ala
NM_001371712.1:c.584G>C	NP_001358641.1:p.Gly195Ala