Canonical Allele Identifier: CA346717999

Gene: TTC7A STPG4

Linked Data

• MyVariant Identifiers: chr2:g.47300955C>A (hg19) ; chr2:g.47073816C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47073816C>A , CM000664.2:g.47073816C>A	GRCh38
NC_000002.11:g.47300955C>A , CM000664.1:g.47300955C>A	GRCh37
NC_000002.10:g.47154459C>A	NCBI36
NG_034143.1:g.162688C>A
NG_034143.2:g.162688C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000698500.1:n.4303C>A (TTC7A)
ENST00000698503.1:n.2476C>A (TTC7A)
ENST00000319190.11:c.2470C>A (TTC7A) MANE Select	ENSP00000316699.5:p.Gln824Lys
ENST00000651101.1:n.1068C>A (TTC7A)
ENST00000651415.1:n.1261C>A (TTC7A)
ENST00000652236.1:n.1171C>A (TTC7A)
ENST00000652568.1:n.1143C>A (TTC7A)
ENST00000319190.9:c.2470C>A (TTC7A)	ENSP00000316699.5:p.Gln824Lys
ENST00000394850.6:c.2542C>A (TTC7A)	ENSP00000378320.2:p.Gln848Lys
ENST00000409245.5:c.2368C>A (TTC7A)	ENSP00000386307.1:p.Gln790Lys
ENST00000409825.5:c.2418C>A (TTC7A)
ENST00000422269.1:c.787-7679G>T
ENST00000441914.5:c.2311C>A (TTC7A)
ENST00000464527.2:n.399-7679G>T (STPG4)
ENST00000482548.1:n.402-5260G>T (STPG4)
ENST00000484061.5:n.1577C>A (TTC7A)
ENST00000491786.5:n.1874C>A (TTC7A)
ENST00000496939.1:n.416-26897G>T (STPG4)
NM_001288951.1:c.2542C>A (TTC7A)	NP_001275880.1:p.Gln848Lys
NM_001288953.1:c.2368C>A (TTC7A)	NP_001275882.1:p.Gln790Lys
NM_001288955.1:c.1408C>A (TTC7A)	NP_001275884.1:p.Gln470Lys
NM_020458.3:c.2470C>A (TTC7A)	NP_065191.2:p.Gln824Lys
XM_005264439.2:c.2113C>A (TTC7A)	XP_005264496.1:p.Gln705Lys
XM_011532998.1:c.2113C>A (TTC7A)	XP_011531300.1:p.Gln705Lys
XM_011533000.1:c.1690C>A (TTC7A)	XP_011531302.1:p.Gln564Lys
XM_011533001.1:c.1423C>A (TTC7A)	XP_011531303.1:p.Gln475Lys
XM_005264439.4:c.2113C>A (TTC7A)	XP_005264496.1:p.Gln705Lys
XM_011532998.3:c.2113C>A (TTC7A)	XP_011531300.1:p.Gln705Lys
XM_011533000.3:c.1690C>A (TTC7A)	XP_011531302.1:p.Gln564Lys
XM_011533001.3:c.1423C>A (TTC7A)	XP_011531303.1:p.Gln475Lys
XM_017004524.1:c.2353C>A (TTC7A)	XP_016860013.1:p.Gln785Lys
XM_017004525.1:c.2302C>A (TTC7A)	XP_016860014.1:p.Gln768Lys
XM_017004526.1:c.2221C>A (TTC7A)	XP_016860015.1:p.Gln741Lys
XM_024453013.1:c.1435C>A (TTC7A)	XP_024308781.1:p.Gln479Lys
NM_020458.4:c.2470C>A (TTC7A) MANE Select	NP_065191.2:p.Gln824Lys
NM_001288951.2:c.2542C>A (TTC7A)	NP_001275880.1:p.Gln848Lys
NM_001288953.2:c.2368C>A (TTC7A)	NP_001275882.1:p.Gln790Lys
NM_001288955.2:c.1408C>A (TTC7A)	NP_001275884.1:p.Gln470Lys