Canonical Allele Identifier: CA2154557137

Gene: TTC7B

Linked Data

• dbSNP Id: rs1890275859

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.90555803_90555805del , CM000676.2:g.90555803_90555805del	GRCh38
NC_000014.8:g.91022147_91022149del , CM000676.1:g.91022147_91022149del	GRCh37
NC_000014.7:g.90091900_90091902del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000328459.11:c.2311-14214_2311-14212del MANE Select	ENSP00000336127.4:n.2311-14214_2311-14212...
ENST00000328459.10:c.2311-14214_2311-14212del	ENSP00000336127.4:n.2311-14214_2311-14212...
ENST00000553972.5:c.772-14214_772-14212del	ENSP00000451440.1:n.772-14214_772-14212de...
ENST00000554654.5:n.900-14214_900-14212del
ENST00000555005.5:c.1729-14214_1729-14212del	ENSP00000451825.1:n.1729-14214_1729-14212...
ENST00000555894.5:c.335-14214_335-14212del	ENSP00000452594.1:n.335-14214_335-14212de...
ENST00000557292.1:c.593-14214_593-14212del
NM_001010854.1:c.2311-14214_2311-14212del	NP_001010854.1:n.2311-14214_2311-14212del...
XM_005267367.1:c.1750-14214_1750-14212del	XP_005267424.1:n.1750-14214_1750-14212del...
XM_011536497.1:c.2218-14214_2218-14212del	XP_011534799.1:n.2218-14214_2218-14212del...
XM_011536498.1:c.1750-14214_1750-14212del	XP_011534800.1:n.1750-14214_1750-14212del...
NM_001320421.1:c.2056-14214_2056-14212del	NP_001307350.1:n.2056-14214_2056-14212del...
XM_017021044.2:c.2524-14214_2524-14212del	XP_016876533.1:n.2524-14214_2524-14212del...
XM_017021045.2:c.2362-14214_2362-14212del	XP_016876534.1:n.2362-14214_2362-14212del...
XM_017021046.1:c.2005-14214_2005-14212del	XP_016876535.1:n.2005-14214_2005-14212del...
XM_017021047.1:c.1537-14214_1537-14212del	XP_016876536.1:n.1537-14214_1537-14212del...
NM_001010854.2:c.2311-14214_2311-14212del MANE Select	NP_001010854.1:n.2311-14214_2311-14212del...
NM_001320421.2:c.2056-14214_2056-14212del	NP_001307350.1:n.2056-14214_2056-14212del...
NM_001401365.1:c.2524-14214_2524-14212del	NP_001388294.1:n.2524-14214_2524-14212del...