Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.21852548G>C , CM000669.2:g.21852548G>C | GRCh38 |
| NC_000007.13:g.21892166G>C , CM000669.1:g.21892166G>C | GRCh37 |
| NC_000007.12:g.21858691G>C | NCBI36 |
| NG_012886.2:g.314334G>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001277115.2:c.10978G>C MANE Select | NP_001264044.1:p.Ala3660Pro |
| ENST00000409508.8:c.10978G>C MANE Select | ENSP00000475939.1:p.Ala3660Pro |
| NM_001277115.1:c.10978G>C | NP_001264044.1:p.Ala3660Pro |
| ENST00000328843.10:c.10999G>C | ENSP00000330671.7:p.Ala3667Pro |
| ENST00000409508.7:c.10978G>C | ENSP00000475939.1:p.Ala3660Pro |
| ENST00000421290.1:n.161G>C | |
| ENST00000607413.5:n.241G>C | |
| ENST00000620169.4:c.10999G>C | ENSP00000481693.1:p.Ala3667Pro |