Canonical Allele Identifier: CA346718047

Gene: TTC7A STPG4

Linked Data

• MyVariant Identifiers: chr2:g.47300977C>A (hg19) ; chr2:g.47073838C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47073838C>A , CM000664.2:g.47073838C>A	GRCh38
NC_000002.11:g.47300977C>A , CM000664.1:g.47300977C>A	GRCh37
NC_000002.10:g.47154481C>A	NCBI36
NG_034143.1:g.162710C>A
NG_034143.2:g.162710C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698500.1:n.4325C>A (TTC7A)
ENST00000698503.1:n.2498C>A (TTC7A)
ENST00000319190.11:c.2492C>A (TTC7A) MANE Select	ENSP00000316699.5:p.Ala831Asp
ENST00000651101.1:n.1090C>A (TTC7A)
ENST00000651415.1:n.1283C>A (TTC7A)
ENST00000652236.1:n.1193C>A (TTC7A)
ENST00000652568.1:n.1165C>A (TTC7A)
ENST00000319190.9:c.2492C>A (TTC7A)	ENSP00000316699.5:p.Ala831Asp
ENST00000394850.6:c.2564C>A (TTC7A)	ENSP00000378320.2:p.Ala855Asp
ENST00000409245.5:c.2390C>A (TTC7A)	ENSP00000386307.1:p.Ala797Asp
ENST00000409825.5:c.2440C>A (TTC7A)
ENST00000422269.1:c.787-7701G>T
ENST00000441914.5:c.2333C>A (TTC7A)
ENST00000464527.2:n.399-7701G>T (STPG4)
ENST00000482548.1:n.402-5282G>T (STPG4)
ENST00000484061.5:n.1599C>A (TTC7A)
ENST00000491786.5:n.1896C>A (TTC7A)
ENST00000496939.1:n.416-26919G>T (STPG4)
NM_001288951.1:c.2564C>A (TTC7A)	NP_001275880.1:p.Ala855Asp
NM_001288953.1:c.2390C>A (TTC7A)	NP_001275882.1:p.Ala797Asp
NM_001288955.1:c.1430C>A (TTC7A)	NP_001275884.1:p.Ala477Asp
NM_020458.3:c.2492C>A (TTC7A)	NP_065191.2:p.Ala831Asp
XM_005264439.2:c.2135C>A (TTC7A)	XP_005264496.1:p.Ala712Asp
XM_011532998.1:c.2135C>A (TTC7A)	XP_011531300.1:p.Ala712Asp
XM_011533000.1:c.1712C>A (TTC7A)	XP_011531302.1:p.Ala571Asp
XM_011533001.1:c.1445C>A (TTC7A)	XP_011531303.1:p.Ala482Asp
XM_005264439.4:c.2135C>A (TTC7A)	XP_005264496.1:p.Ala712Asp
XM_011532998.3:c.2135C>A (TTC7A)	XP_011531300.1:p.Ala712Asp
XM_011533000.3:c.1712C>A (TTC7A)	XP_011531302.1:p.Ala571Asp
XM_011533001.3:c.1445C>A (TTC7A)	XP_011531303.1:p.Ala482Asp
XM_017004524.1:c.2375C>A (TTC7A)	XP_016860013.1:p.Ala792Asp
XM_017004525.1:c.2324C>A (TTC7A)	XP_016860014.1:p.Ala775Asp
XM_017004526.1:c.2243C>A (TTC7A)	XP_016860015.1:p.Ala748Asp
XM_024453013.1:c.1457C>A (TTC7A)	XP_024308781.1:p.Ala486Asp
NM_020458.4:c.2492C>A (TTC7A) MANE Select	NP_065191.2:p.Ala831Asp
NM_001288951.2:c.2564C>A (TTC7A)	NP_001275880.1:p.Ala855Asp
NM_001288953.2:c.2390C>A (TTC7A)	NP_001275882.1:p.Ala797Asp
NM_001288955.2:c.1430C>A (TTC7A)	NP_001275884.1:p.Ala477Asp