Canonical Allele Identifier: CA467490603
Gene: DOLK HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.131708347G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.128946068G>T , CM000671.2:g.128946068G>T GRCh38
NC_000009.11:g.131708347G>T , CM000671.1:g.131708347G>T GRCh37
NC_000009.10:g.130748168G>T NCBI36
NG_017009.1:g.6666C>A , LRG_744:g.6666C>A
NG_033111.1:g.3376G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372586.4:c.1236C>A MANE Select ENSP00000361667.3:p.Leu412=
ENST00000372586.3:c.1236C>A ENSP00000361667.3:p.Leu412=
ENST00000482796.1:c.39-3121G>T ENSP00000417556.2:n.39-3121G>T
NM_014908.3:c.1236C>A , LRG_744t1:c.1236C>A NP_055723.1:p.Leu412=
NM_014908.4:c.1236C>A MANE Select NP_055723.1:p.Leu412=