Canonical Allele Identifier: CA1585274675
Gene: SPOCK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.137111657A= , CM000667.2:g.137111657A= GRCh38
NC_000005.9:g.136447346A= , CM000667.1:g.136447346A= GRCh37
NC_000005.8:g.136475245A= NCBI36
NG_034127.1:g.392673T=

Transcript Alleles

HGVS Amino-acid change
ENST00000394945.6:c.474+778T= MANE Select ENSP00000378401.1:n.474+778T=
ENST00000282223.11:c.288+778T= ENSP00000282223.9:n.288+778T=
ENST00000394945.5:c.474+778T= ENSP00000378401.1:n.474+778T=
ENST00000510689.5:c.39+778T= ENSP00000421677.1:n.39+778T=
ENST00000635347.1:n.447+778T=
NM_004598.3:c.474+778T= NP_004589.1:n.474+778T=
NM_004598.4:c.474+778T= MANE Select NP_004589.1:n.474+778T=