Canonical Allele Identifier: CA411939978

Gene: TTC38

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.46281617A>G , CM000684.2:g.46281617A>G	GRCh38
NC_000022.10:g.46677514A>G , CM000684.1:g.46677514A>G	GRCh37
NC_000022.9:g.45056178A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_017931.4:c.634A>G MANE Select	NP_060401.3:p.Thr212Ala
ENST00000381031.8:c.634A>G MANE Select	ENSP00000370419.3:p.Thr212Ala
NM_017931.2:c.634A>G	NP_060401.2:p.Thr212Ala
NM_017931.3:c.634A>G	NP_060401.2:p.Thr212Ala
ENST00000381031.7:c.634A>G	ENSP00000370419.3:p.Thr212Ala
ENST00000422713.1:c.486A>G
XM_011530259.1:c.439A>G	XP_011528561.1:p.Thr147Ala
XM_011530261.1:c.634A>G	XP_011528563.1:p.Thr212Ala
XR_001755257.1:n.817A>G
XR_001755258.2:n.690A>G
XR_001755259.2:n.690A>G
XR_001755260.2:n.690A>G
XR_002958710.1:n.2337A>G
XR_244380.3:n.710A>G
XR_244380.4:n.690A>G