Canonical Allele Identifier: CA399478901

Gene: HAP1

Linked Data

• gnomAD v4: 17-41727099-T-C
• MyVariant Identifiers: chr17:g.39883351T>C (hg19) ; chr17:g.41727099T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41727099T>C , CM000679.2:g.41727099T>C	GRCh38
NC_000017.10:g.39883351T>C , CM000679.1:g.39883351T>C	GRCh37
NC_000017.9:g.37136877T>C	NCBI36
NG_009090.2:g.64614A>G , LRG_401:g.64614A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347901.9:c.1321A>G MANE Select	ENSP00000334002.4:p.Thr441Ala
ENST00000310778.5:c.1477A>G	ENSP00000309392.5:p.Thr493Ala
ENST00000341193.9:c.1270A>G	ENSP00000343170.5:p.Thr424Ala
ENST00000347901.8:c.1321A>G	ENSP00000334002.4:p.Thr441Ala
ENST00000393939.6:c.1246A>G	ENSP00000377513.2:p.Thr416Ala
NM_001079870.1:c.1270A>G	NP_001073339.1:p.Thr424Ala
NM_001079871.1:c.1246A>G	NP_001073340.1:p.Thr416Ala
NM_177977.2:c.1321A>G	NP_817084.2:p.Thr441Ala
NM_001367459.1:c.1417A>G	NP_001354388.1:p.Thr473Ala
NM_001367460.1:c.1381A>G	NP_001354389.1:p.Thr461Ala
NM_001367461.1:c.1246A>G	NP_001354390.1:p.Thr416Ala
NM_001367462.1:c.1246A>G	NP_001354391.1:p.Thr416Ala
NM_177977.3:c.1321A>G MANE Select	NP_817084.2:p.Thr441Ala