HGVS | Genome Assembly |
---|---|
NC_000002.12:g.135817349_135817357del , CM000664.2:g.135817349_135817357del | GRCh38 |
NC_000002.11:g.136574919_136574927del , CM000664.1:g.136574919_136574927del | GRCh37 |
NC_000002.10:g.136291389_136291397del | NCBI36 |
NG_008104.2:g.42813_42821del , LRG_338:g.42813_42821del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000264162.7:c.1691_1699del MANE Select | ENSP00000264162.2:p.Gly564_Ser567delinsAl... | |
ENST00000264162.6:c.1691_1699del | ENSP00000264162.2:p.Gly564_Ser567delinsAl... | |
NM_002299.2:c.1691_1699del , LRG_338t1:c.1691_1699del | NP_002290.2:p.Gly564_Ser567delinsAla | |
NM_002299.3:c.1691_1699del | NP_002290.2:p.Gly564_Ser567delinsAla | |
XM_017004088.2:c.1691_1699del | XP_016859577.1:p.Gly564_Ser567delinsAla | |
NM_002299.4:c.1691_1699del MANE Select | NP_002290.2:p.Gly564_Ser567delinsAla |