Canonical Allele Identifier: CA323355567

Gene: TTC28

Linked Data

• dbSNP Id: rs12166475
• gnomAD v2: 22-28860167-T-C
• gnomAD v3: 22-28464179-T-C
• gnomAD v4: 22-28464179-T-C
• MyVariant Identifiers: chr22:g.28860167T>C (hg19) ; chr22:g.28464179T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.28464179T>C , CM000684.2:g.28464179T>C	GRCh38
NC_000022.10:g.28860167T>C , CM000684.1:g.28860167T>C	GRCh37
NC_000022.9:g.27190167T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000397906.7:c.382-157536A>G MANE Select	ENSP00000381003.2:n.382-157536A>G
ENST00000397906.6:c.382-157536A>G	ENSP00000381003.2:n.382-157536A>G
NM_001145418.1:c.382-157536A>G	NP_001138890.1:n.382-157536A>G
XM_005261405.2:c.382-157536A>G	XP_005261462.1:n.382-157536A>G
XM_011530018.1:c.304-157536A>G	XP_011528320.1:n.304-157536A>G
XM_011530019.1:c.382-157536A>G	XP_011528321.1:n.382-157536A>G
XM_011530020.1:c.382-157536A>G	XP_011528322.1:n.382-157536A>G
XM_011530021.1:c.382-157536A>G	XP_011528323.1:n.382-157536A>G
XM_011530022.1:c.382-157536A>G	XP_011528324.1:n.382-157536A>G
XM_011530018.3:c.304-157536A>G	XP_011528320.1:n.304-157536A>G
XM_011530019.2:c.382-157536A>G	XP_011528321.1:n.382-157536A>G
XM_011530021.3:c.382-157536A>G	XP_011528323.1:n.382-157536A>G
XM_017028673.2:c.292-157536A>G	XP_016884162.1:n.292-157536A>G
NM_001145418.2:c.382-157536A>G MANE Select	NP_001138890.1:n.382-157536A>G
NM_001393403.1:c.382-157536A>G	NP_001380332.1:n.382-157536A>G