Canonical Allele Identifier: CA2154557149

Gene: TTC7B

Linked Data

• dbSNP Id: rs1890277207

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.90555852del , CM000676.2:g.90555852del	GRCh38
NC_000014.8:g.91022196del , CM000676.1:g.91022196del	GRCh37
NC_000014.7:g.90091949del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000328459.11:c.2311-14263del MANE Select	ENSP00000336127.4:n.2311-14263del
ENST00000328459.10:c.2311-14263del	ENSP00000336127.4:n.2311-14263del
ENST00000553972.5:c.772-14263del	ENSP00000451440.1:n.772-14263del
ENST00000554654.5:n.900-14263del
ENST00000555005.5:c.1729-14263del	ENSP00000451825.1:n.1729-14263del
ENST00000555894.5:c.335-14263del	ENSP00000452594.1:n.335-14263del
ENST00000557292.1:c.593-14263del
NM_001010854.1:c.2311-14263del	NP_001010854.1:n.2311-14263del
XM_005267367.1:c.1750-14263del	XP_005267424.1:n.1750-14263del
XM_011536497.1:c.2218-14263del	XP_011534799.1:n.2218-14263del
XM_011536498.1:c.1750-14263del	XP_011534800.1:n.1750-14263del
NM_001320421.1:c.2056-14263del	NP_001307350.1:n.2056-14263del
XM_017021044.2:c.2524-14263del	XP_016876533.1:n.2524-14263del
XM_017021045.2:c.2362-14263del	XP_016876534.1:n.2362-14263del
XM_017021046.1:c.2005-14263del	XP_016876535.1:n.2005-14263del
XM_017021047.1:c.1537-14263del	XP_016876536.1:n.1537-14263del
NM_001010854.2:c.2311-14263del MANE Select	NP_001010854.1:n.2311-14263del
NM_001320421.2:c.2056-14263del	NP_001307350.1:n.2056-14263del
NM_001401365.1:c.2524-14263del	NP_001388294.1:n.2524-14263del