Canonical Allele Identifier: CA2242851093
Community Standard Title: NM_016823.4(CRK):c.778-6150C=
Gene: CRK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.1429800G= , CM000679.2:g.1429800G= GRCh38
NC_000017.10:g.1333094G= , CM000679.1:g.1333094G= GRCh37
NC_000017.9:g.1279844G= NCBI36
NG_029008.1:g.31451C=

Transcript Alleles

HGVS Amino-acid Change
NM_016823.4:c.778-6150C= MANE Select NP_058431.2:n.778-6150C=
ENST00000300574.3:c.778-6150C= MANE Select ENSP00000300574.2:n.778-6150C=
NM_005206.4:c.608-6150C= NP_005197.3:n.608-6150C=
NM_005206.5:c.608-6150C= NP_005197.3:n.608-6150C=
NM_016823.3:c.778-6150C= NP_058431.2:n.778-6150C=
ENST00000300574.2:c.778-6150C= ENSP00000300574.2:n.778-6150C=
ENST00000398970.5:c.608-6150C= ENSP00000381942.5:n.608-6150C=
ENST00000572145.1:n.577-6150C=
ENST00000574295.1:c.400-6615C= ENSP00000459505.1:n.400-6615C=