Canonical Allele Identifier: CA393754386
Community Standard Title: NM_198525.3(KIF7):c.3518-1G>C

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89629123C>G , CM000677.2:g.89629123C>G GRCh38
NC_000015.9:g.90172354C>G , CM000677.1:g.90172354C>G GRCh37
NC_000015.8:g.87973358C>G NCBI36
NG_030338.1:g.31329G>C

Transcript Alleles

HGVS Amino-acid Change
NM_198525.3:c.3518-1G>C (KIF7) MANE Select NP_940927.2:n.3518-1G>C
ENST00000394412.8:c.3518-1G>C (KIF7) MANE Select ENSP00000377934.3:n.3518-1G>C
NM_198525.2:c.3518-1G>C (KIF7) NP_940927.2:n.3518-1G>C
ENST00000394412.7:c.3518-1G>C (KIF7) ENSP00000377934.3:n.3518-1G>C
ENST00000561095.1:c.741-307C>G (TICRR)
ENST00000677187.1:n.1192-1G>C (KIF7)
ENST00000696512.1:c.3641-1G>C (KIF7) ENSP00000512678.1:n.3641-1G>C
XM_005254902.2:c.3518-1G>C (KIF7) XP_005254959.1:n.3518-1G>C
XM_011521531.1:c.3641-1G>C (KIF7) XP_011519833.1:n.3641-1G>C
XM_011521531.2:c.3641-1G>C (KIF7) XP_011519833.1:n.3641-1G>C
XM_011521532.1:c.3638-1G>C (KIF7) XP_011519834.1:n.3638-1G>C
XM_011521533.1:c.3638-1G>C (KIF7) XP_011519835.1:n.3638-1G>C
XM_011521534.1:c.3641-1G>C (KIF7) XP_011519836.1:n.3641-1G>C
XM_011521535.1:c.3641-1G>C (KIF7) XP_011519837.1:n.3641-1G>C
XM_011521536.1:c.3641-1G>C (KIF7) XP_011519838.1:n.3641-1G>C