Canonical Allele Identifier: CA2694293712
Gene: TIMM8A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101348474_101348475insTCCTT , CM000685.2:g.101348474_101348475insTCCTT GRCh38
NC_000023.10:g.100603462_100603463insTCCTT , CM000685.1:g.100603462_100603463insTCCTT GRCh37
NC_000023.9:g.100490118_100490119insTCCTT NCBI36
NG_009616.1:g.42750_42751insAAGGA , LRG_128:g.42750_42751insAAGGA
NG_011734.1:g.5495_5496insAAGGA

Transcript Alleles

HGVS Amino-acid change
ENST00000372902.4:c.132+58_132+59insAAGGA MANE Select ENSP00000361993.3:n.132+58_132+59insAAGGA...
ENST00000644112.2:c.132+58_132+59insAAGGA ENSP00000494385.1:n.132+58_132+59insAAGGA...
ENST00000645279.1:c.132+58_132+59insAAGGA ENSP00000494239.1:n.132+58_132+59insAAGGA...
ENST00000647480.1:n.101_102insAAGGA
ENST00000372902.3:c.132+58_132+59insAAGGA ENSP00000361993.3:n.132+58_132+59insAAGGA...
ENST00000480575.1:n.217+58_217+59insAAGGA
NM_001145951.1:c.132+58_132+59insAAGGA NP_001139423.1:n.132+58_132+59insAAGGA
NM_004085.3:c.132+58_132+59insAAGGA NP_004076.1:n.132+58_132+59insAAGGA
NM_004085.4:c.132+58_132+59insAAGGA MANE Select NP_004076.1:n.132+58_132+59insAAGGA
NM_001145951.2:c.132+58_132+59insAAGGA NP_001139423.1:n.132+58_132+59insAAGGA