Canonical Allele Identifier: CA346718033

Gene: TTC7A STPG4

Linked Data

• MyVariant Identifiers: chr2:g.47300970A>G (hg19) ; chr2:g.47073831A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47073831A>G , CM000664.2:g.47073831A>G	GRCh38
NC_000002.11:g.47300970A>G , CM000664.1:g.47300970A>G	GRCh37
NC_000002.10:g.47154474A>G	NCBI36
NG_034143.1:g.162703A>G
NG_034143.2:g.162703A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698500.1:n.4318A>G (TTC7A)
ENST00000698503.1:n.2491A>G (TTC7A)
ENST00000319190.11:c.2485A>G (TTC7A) MANE Select	ENSP00000316699.5:p.Asn829Asp
ENST00000651101.1:n.1083A>G (TTC7A)
ENST00000651415.1:n.1276A>G (TTC7A)
ENST00000652236.1:n.1186A>G (TTC7A)
ENST00000652568.1:n.1158A>G (TTC7A)
ENST00000319190.9:c.2485A>G (TTC7A)	ENSP00000316699.5:p.Asn829Asp
ENST00000394850.6:c.2557A>G (TTC7A)	ENSP00000378320.2:p.Asn853Asp
ENST00000409245.5:c.2383A>G (TTC7A)	ENSP00000386307.1:p.Asn795Asp
ENST00000409825.5:c.2433A>G (TTC7A)
ENST00000422269.1:c.787-7694T>C
ENST00000441914.5:c.2326A>G (TTC7A)
ENST00000464527.2:n.399-7694T>C (STPG4)
ENST00000482548.1:n.402-5275T>C (STPG4)
ENST00000484061.5:n.1592A>G (TTC7A)
ENST00000491786.5:n.1889A>G (TTC7A)
ENST00000496939.1:n.416-26912T>C (STPG4)
NM_001288951.1:c.2557A>G (TTC7A)	NP_001275880.1:p.Asn853Asp
NM_001288953.1:c.2383A>G (TTC7A)	NP_001275882.1:p.Asn795Asp
NM_001288955.1:c.1423A>G (TTC7A)	NP_001275884.1:p.Asn475Asp
NM_020458.3:c.2485A>G (TTC7A)	NP_065191.2:p.Asn829Asp
XM_005264439.2:c.2128A>G (TTC7A)	XP_005264496.1:p.Asn710Asp
XM_011532998.1:c.2128A>G (TTC7A)	XP_011531300.1:p.Asn710Asp
XM_011533000.1:c.1705A>G (TTC7A)	XP_011531302.1:p.Asn569Asp
XM_011533001.1:c.1438A>G (TTC7A)	XP_011531303.1:p.Asn480Asp
XM_005264439.4:c.2128A>G (TTC7A)	XP_005264496.1:p.Asn710Asp
XM_011532998.3:c.2128A>G (TTC7A)	XP_011531300.1:p.Asn710Asp
XM_011533000.3:c.1705A>G (TTC7A)	XP_011531302.1:p.Asn569Asp
XM_011533001.3:c.1438A>G (TTC7A)	XP_011531303.1:p.Asn480Asp
XM_017004524.1:c.2368A>G (TTC7A)	XP_016860013.1:p.Asn790Asp
XM_017004525.1:c.2317A>G (TTC7A)	XP_016860014.1:p.Asn773Asp
XM_017004526.1:c.2236A>G (TTC7A)	XP_016860015.1:p.Asn746Asp
XM_024453013.1:c.1450A>G (TTC7A)	XP_024308781.1:p.Asn484Asp
NM_020458.4:c.2485A>G (TTC7A) MANE Select	NP_065191.2:p.Asn829Asp
NM_001288951.2:c.2557A>G (TTC7A)	NP_001275880.1:p.Asn853Asp
NM_001288953.2:c.2383A>G (TTC7A)	NP_001275882.1:p.Asn795Asp
NM_001288955.2:c.1423A>G (TTC7A)	NP_001275884.1:p.Asn475Asp