HGVS | Genome Assembly |
---|---|
NC_000014.9:g.75005820_75005829dup , CM000676.2:g.75005820_75005829dup | GRCh38 |
NC_000014.8:g.75472523_75472532dup , CM000676.1:g.75472523_75472532dup | GRCh37 |
NC_000014.7:g.74542276_74542285dup | NCBI36 |
NG_013333.1:g.7912_7921dup |
HGVS | Amino-acid change | |
---|---|---|
ENST00000266126.10:c.598-46_598-37dup MANE Select | ENSP00000266126.5:n.598-46_598-37dup | |
ENST00000266126.9:c.598-46_598-37dup | ENSP00000266126.5:n.598-46_598-37dup | |
ENST00000553401.5:c.571-21_571-12dup | ENSP00000451681.1:n.571-21_571-12dup | |
ENST00000556028.5:c.598-77_598-68dup | ENSP00000452311.1:n.598-77_598-68dup | |
NM_014239.3:c.598-46_598-37dup | NP_055054.1:n.598-46_598-37dup | |
NM_014239.4:c.598-46_598-37dup MANE Select | NP_055054.1:n.598-46_598-37dup |