Canonical Allele Identifier: CA2679182214
Gene: HCRTR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.55248613_55248614insTATTTTCTTTGTTGAGTGA , CM000668.2:g.55248613_55248614insTATTTTCTTTGTTGAGTGA GRCh38
NC_000006.11:g.55113411_55113412insTATTTTCTTTGTTGAGTGA , CM000668.1:g.55113411_55113412insTATTTTCTTTGTTGAGTGA GRCh37
NC_000006.10:g.55221370_55221371insTATTTTCTTTGTTGAGTGA NCBI36
NG_012447.1:g.79341_79342insTATTTTCTTTGTTGAGTGA
NG_012447.2:g.147154_147155insTATTTTCTTTGTTGAGTGA

Transcript Alleles

HGVS Amino-acid change
ENST00000370862.4:c.224-26_224-25insTATTTTCTTTGTTGAGTGA MANE Select ENSP00000359899.3:n.224-26_224-25insTATTT...
ENST00000370862.3:c.224-26_224-25insTATTTTCTTTGTTGAGTGA ENSP00000359899.3:n.224-26_224-25insTATTT...
ENST00000615358.4:c.224-26_224-25insTATTTTCTTTGTTGAGTGA ENSP00000477548.1:n.224-26_224-25insTATTT...
NM_001526.3:c.224-26_224-25insTATTTTCTTTGTTGAGTGA NP_001517.2:n.224-26_224-25insTATTTTCTTTG...
XM_011514542.1:c.29-26_29-25insTATTTTCTTTGTTGAGTGA XP_011512844.1:n.29-26_29-25insTATTTTCTTT...
NM_001526.4:c.224-26_224-25insTATTTTCTTTGTTGAGTGA NP_001517.2:n.224-26_224-25insTATTTTCTTTG...
XM_017010798.1:c.224-26_224-25insTATTTTCTTTGTTGAGTGA XP_016866287.1:n.224-26_224-25insTATTTTCT...
NM_001384272.1:c.224-26_224-25insTATTTTCTTTGTTGAGTGA MANE Select NP_001371201.1:n.224-26_224-25insTATTTTCT...
NM_001526.5:c.224-26_224-25insTATTTTCTTTGTTGAGTGA NP_001517.2:n.224-26_224-25insTATTTTCTTTG...