Canonical Allele Identifier: CA10639555
Community Standard Title: NM_001004334.4(GPR179):c.991+4T>C
Gene: GPR179 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.38337629A>G , CM000679.2:g.38337629A>G GRCh38
NC_000017.9:g.33747038A>G NCBI36
NG_032655.2:g.11182T>C

Transcript Alleles

HGVS Amino-acid Change
NM_001004334.4:c.991+4T>C MANE Select NP_001004334.3:n.991+4T>C
ENST00000616987.5:c.991+4T>C MANE Select ENSP00000483469.2:n.991+4T>C
NM_001004334.3:c.991+4T>C NP_001004334.3:n.991+4T>C
ENST00000616987.4:c.991+4T>C ENSP00000483469.1:n.991+4T>C
ENST00000621958.1:c.994+4T>C ENSP00000480024.1:n.994+4T>C