Canonical Allele Identifier: CA7727805

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89630413T>A , CM000677.2:g.89630413T>A GRCh38
NC_000015.9:g.90173644T>A , CM000677.1:g.90173644T>A GRCh37
NC_000015.8:g.87974648T>A NCBI36
NG_030338.1:g.30039A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696512.1:c.3315A>T (KIF7) ENSP00000512678.1:p.Thr1105=
ENST00000394412.8:c.3192A>T (KIF7) MANE Select ENSP00000377934.3:p.Thr1064=
ENST00000677187.1:n.866A>T (KIF7)
ENST00000394412.7:c.3192A>T (KIF7) ENSP00000377934.3:p.Thr1064=
ENST00000561095.1:c.1724T>A (TICRR)
NM_198525.2:c.3192A>T (KIF7) NP_940927.2:p.Thr1064=
XM_005254902.2:c.3192A>T (KIF7) XP_005254959.1:p.Thr1064=
XM_011521531.1:c.3315A>T (KIF7) XP_011519833.1:p.Thr1105=
XM_011521532.1:c.3312A>T (KIF7) XP_011519834.1:p.Thr1104=
XM_011521533.1:c.3312A>T (KIF7) XP_011519835.1:p.Thr1104=
XM_011521534.1:c.3315A>T (KIF7) XP_011519836.1:p.Thr1105=
XM_011521535.1:c.3315A>T (KIF7) XP_011519837.1:p.Thr1105=
XM_011521536.1:c.3315A>T (KIF7) XP_011519838.1:p.Thr1105=
XM_011521531.2:c.3315A>T (KIF7) XP_011519833.1:p.Thr1105=
NM_198525.3:c.3192A>T (KIF7) MANE Select NP_940927.2:p.Thr1064=