Canonical Allele Identifier: CA15150197

Gene: TTC7A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47029663G>C , CM000664.2:g.47029663G>C	GRCh38
NC_000002.11:g.47256802G>C , CM000664.1:g.47256802G>C	GRCh37
NC_000002.10:g.47110306G>C	NCBI36
NG_034143.1:g.118535G>C
NG_034143.2:g.118535G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_020458.4:c.1802+279G>C MANE Select	NP_065191.2:n.1802+279G>C
ENST00000319190.11:c.1802+279G>C MANE Select	ENSP00000316699.5:n.1802+279G>C
NM_001288951.1:c.1802+279G>C	NP_001275880.1:n.1802+279G>C
NM_001288951.2:c.1802+279G>C	NP_001275880.1:n.1802+279G>C
NM_001288953.1:c.1700+279G>C	NP_001275882.1:n.1700+279G>C
NM_001288953.2:c.1700+279G>C	NP_001275882.1:n.1700+279G>C
NM_001288955.1:c.740+279G>C	NP_001275884.1:n.740+279G>C
NM_001288955.2:c.740+279G>C	NP_001275884.1:n.740+279G>C
NM_020458.3:c.1802+279G>C	NP_065191.2:n.1802+279G>C
ENST00000319190.9:c.1802+279G>C	ENSP00000316699.5:n.1802+279G>C
ENST00000394850.6:c.1802+279G>C	ENSP00000378320.2:n.1802+279G>C
ENST00000409245.5:c.1700+279G>C	ENSP00000386307.1:n.1700+279G>C
ENST00000409825.5:c.1750+279G>C
ENST00000440051.1:c.609+279G>C
ENST00000441914.5:c.1643+279G>C
ENST00000461601.5:n.2127+279G>C
ENST00000484061.5:n.909+279G>C
ENST00000491786.5:n.1206+279G>C
ENST00000651101.1:n.750+279G>C
ENST00000651415.1:n.593+279G>C
ENST00000652236.1:n.503+279G>C
ENST00000652568.1:n.475+279G>C
ENST00000698500.1:n.3635+279G>C
ENST00000698503.1:n.1808+279G>C
ENST00000698504.1:n.71+279G>C
XM_005264439.2:c.1445+279G>C	XP_005264496.1:n.1445+279G>C
XM_005264439.4:c.1445+279G>C	XP_005264496.1:n.1445+279G>C
XM_011532998.1:c.1445+279G>C	XP_011531300.1:n.1445+279G>C
XM_011532998.3:c.1445+279G>C	XP_011531300.1:n.1445+279G>C
XM_011532999.1:c.1802+279G>C	XP_011531301.1:n.1802+279G>C
XM_011532999.2:c.1802+279G>C	XP_011531301.1:n.1802+279G>C
XM_011533000.1:c.1022+279G>C	XP_011531302.1:n.1022+279G>C
XM_011533000.3:c.1022+279G>C	XP_011531302.1:n.1022+279G>C
XM_011533001.1:c.755+279G>C	XP_011531303.1:n.755+279G>C
XM_011533001.3:c.755+279G>C	XP_011531303.1:n.755+279G>C
XM_017004524.1:c.1802+279G>C	XP_016860013.1:n.1802+279G>C
XM_017004525.1:c.1634+279G>C	XP_016860014.1:n.1634+279G>C
XM_017004526.1:c.1553+279G>C	XP_016860015.1:n.1553+279G>C
XM_017004529.1:c.1802+279G>C	XP_016860018.1:n.1802+279G>C
XM_024453013.1:c.767+279G>C	XP_024308781.1:n.767+279G>C
XR_001738853.2:n.2114+279G>C
XR_001738854.1:n.1995+279G>C
XR_939696.1:n.2107+279G>C