HGVS | Genome Assembly |
---|---|
NC_000019.10:g.15186913_15186915dup , CM000681.2:g.15186913_15186915dup | GRCh38 |
NC_000019.9:g.15297724_15297726dup , CM000681.1:g.15297724_15297726dup | GRCh37 |
NC_000019.8:g.15158724_15158726dup | NCBI36 |
NG_009819.1:g.19068_19070dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263388.7:c.1915_1917dup MANE Select | ENSP00000263388.1:p.Asn639_Arg640insAsn | |
ENST00000263388.6:c.1915_1917dup | ENSP00000263388.1:p.Asn639_Arg640insAsn | |
ENST00000601011.1:c.1912_1914dup | ENSP00000473138.1:p.Asn638_Arg639insAsn | |
NM_000435.2:c.1915_1917dup | NP_000426.2:p.Asn639_Arg640insAsn | |
XM_005259924.3:c.1915_1917dup | XP_005259981.1:p.Asn639_Arg640insAsn | |
XM_005259924.4:c.1915_1917dup | XP_005259981.1:p.Asn639_Arg640insAsn | |
NM_000435.3:c.1915_1917dup MANE Select | NP_000426.2:p.Asn639_Arg640insAsn |