Canonical Allele Identifier: CA346718004

Gene: TTC7A STPG4

Linked Data

• MyVariant Identifiers: chr2:g.47300957G>C (hg19) ; chr2:g.47073818G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47073818G>C , CM000664.2:g.47073818G>C	GRCh38
NC_000002.11:g.47300957G>C , CM000664.1:g.47300957G>C	GRCh37
NC_000002.10:g.47154461G>C	NCBI36
NG_034143.1:g.162690G>C
NG_034143.2:g.162690G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000698500.1:n.4305G>C (TTC7A)
ENST00000698503.1:n.2478G>C (TTC7A)
ENST00000319190.11:c.2472G>C (TTC7A) MANE Select	ENSP00000316699.5:p.Gln824His
ENST00000651101.1:n.1070G>C (TTC7A)
ENST00000651415.1:n.1263G>C (TTC7A)
ENST00000652236.1:n.1173G>C (TTC7A)
ENST00000652568.1:n.1145G>C (TTC7A)
ENST00000319190.9:c.2472G>C (TTC7A)	ENSP00000316699.5:p.Gln824His
ENST00000394850.6:c.2544G>C (TTC7A)	ENSP00000378320.2:p.Gln848His
ENST00000409245.5:c.2370G>C (TTC7A)	ENSP00000386307.1:p.Gln790His
ENST00000409825.5:c.2420G>C (TTC7A)
ENST00000422269.1:c.787-7681C>G
ENST00000441914.5:c.2313G>C (TTC7A)
ENST00000464527.2:n.399-7681C>G (STPG4)
ENST00000482548.1:n.402-5262C>G (STPG4)
ENST00000484061.5:n.1579G>C (TTC7A)
ENST00000491786.5:n.1876G>C (TTC7A)
ENST00000496939.1:n.416-26899C>G (STPG4)
NM_001288951.1:c.2544G>C (TTC7A)	NP_001275880.1:p.Gln848His
NM_001288953.1:c.2370G>C (TTC7A)	NP_001275882.1:p.Gln790His
NM_001288955.1:c.1410G>C (TTC7A)	NP_001275884.1:p.Gln470His
NM_020458.3:c.2472G>C (TTC7A)	NP_065191.2:p.Gln824His
XM_005264439.2:c.2115G>C (TTC7A)	XP_005264496.1:p.Gln705His
XM_011532998.1:c.2115G>C (TTC7A)	XP_011531300.1:p.Gln705His
XM_011533000.1:c.1692G>C (TTC7A)	XP_011531302.1:p.Gln564His
XM_011533001.1:c.1425G>C (TTC7A)	XP_011531303.1:p.Gln475His
XM_005264439.4:c.2115G>C (TTC7A)	XP_005264496.1:p.Gln705His
XM_011532998.3:c.2115G>C (TTC7A)	XP_011531300.1:p.Gln705His
XM_011533000.3:c.1692G>C (TTC7A)	XP_011531302.1:p.Gln564His
XM_011533001.3:c.1425G>C (TTC7A)	XP_011531303.1:p.Gln475His
XM_017004524.1:c.2355G>C (TTC7A)	XP_016860013.1:p.Gln785His
XM_017004525.1:c.2304G>C (TTC7A)	XP_016860014.1:p.Gln768His
XM_017004526.1:c.2223G>C (TTC7A)	XP_016860015.1:p.Gln741His
XM_024453013.1:c.1437G>C (TTC7A)	XP_024308781.1:p.Gln479His
NM_020458.4:c.2472G>C (TTC7A) MANE Select	NP_065191.2:p.Gln824His
NM_001288951.2:c.2544G>C (TTC7A)	NP_001275880.1:p.Gln848His
NM_001288953.2:c.2370G>C (TTC7A)	NP_001275882.1:p.Gln790His
NM_001288955.2:c.1410G>C (TTC7A)	NP_001275884.1:p.Gln470His