Canonical Allele Identifier: CA2649105996

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171636099_171636128dup , CM000663.2:g.171636099_171636128dup GRCh38
NC_000001.10:g.171605239_171605268dup , CM000663.1:g.171605239_171605268dup GRCh37
NC_000001.9:g.169871862_169871891dup NCBI36
NG_008859.1:g.21513_21542dup

Transcript Alleles

HGVS Amino-acid change
ENST00000037502.11:c.1319_1348dup (MYOC) MANE Select ENSP00000037502.5:p.Val449_Asn450insSerSe...
ENST00000637303.1:c.235-2531_235-2502dup (MYOCOS) ENSP00000490048.1:n.235-2531_235-2502dup
ENST00000638471.1:c.*657_*686dup (MYOC) ENSP00000491206.1:n.*657_*686dup
ENST00000037502.10:c.1319_1348dup (MYOC) ENSP00000037502.5:p.Val449_Asn450insSerSe...
ENST00000614688.1:c.*283_*312dup (MYOC) ENSP00000478680.1:n.*283_*312dup
NM_000261.1:c.1319_1348dup (MYOC) NP_000252.1:p.Val449_Asn450insSerSerTyrTh...
NM_000261.2:c.1319_1348dup (MYOC) MANE Select NP_000252.1:p.Val449_Asn450insSerSerTyrTh...