Canonical Allele Identifier: CA286793479
Community Standard Title: NM_016823.4(CRK):c.778-6042G>A
Gene: CRK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.1429692C>T , CM000679.2:g.1429692C>T GRCh38
NC_000017.10:g.1332986C>T , CM000679.1:g.1332986C>T GRCh37
NC_000017.9:g.1279736C>T NCBI36
NG_029008.1:g.31559G>A

Transcript Alleles

HGVS Amino-acid Change
NM_016823.4:c.778-6042G>A MANE Select NP_058431.2:n.778-6042G>A
ENST00000300574.3:c.778-6042G>A MANE Select ENSP00000300574.2:n.778-6042G>A
NM_005206.4:c.608-6042G>A NP_005197.3:n.608-6042G>A
NM_005206.5:c.608-6042G>A NP_005197.3:n.608-6042G>A
NM_016823.3:c.778-6042G>A NP_058431.2:n.778-6042G>A
ENST00000300574.2:c.778-6042G>A ENSP00000300574.2:n.778-6042G>A
ENST00000398970.5:c.608-6042G>A ENSP00000381942.5:n.608-6042G>A
ENST00000572145.1:n.577-6042G>A
ENST00000574295.1:c.400-6507G>A ENSP00000459505.1:n.400-6507G>A