Canonical Allele Identifier: CA378208017
Gene: TWNK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.100988883A>C , CM000672.2:g.100988883A>C GRCh38
NC_000010.10:g.102748640A>C , CM000672.1:g.102748640A>C GRCh37
NC_000010.9:g.102738630A>C NCBI36
NG_011646.1:g.3633T>G
NG_012624.1:g.6348A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000311916.8:c.673A>C MANE Select ENSP00000309595.2:p.Lys225Gln
ENST00000370228.2:c.673A>C ENSP00000359248.1:p.Lys225Gln
ENST00000643860.1:c.673A>C ENSP00000494389.1:p.Lys225Gln
ENST00000646226.1:n.59-761A>C
ENST00000311916.6:c.673A>C ENSP00000309595.2:p.Lys225Gln
ENST00000370228.1:c.673A>C ENSP00000359248.1:p.Lys225Gln
ENST00000459764.1:n.87-761A>C
ENST00000473656.5:n.65-761A>C
ENST00000476766.5:n.192-823A>C
NM_001163812.1:c.673A>C NP_001157284.1:p.Lys225Gln
NM_001163813.1:c.-119-761A>C NP_001157285.1:n.-119-761A>C
NM_001163814.1:c.-119-761A>C NP_001157286.1:n.-119-761A>C
NM_021830.4:c.673A>C NP_068602.2:p.Lys225Gln
XM_011539975.1:c.-57-823A>C XP_011538277.1:n.-57-823A>C
XR_945788.1:n.1506A>C
XM_011539975.2:c.-57-823A>C XP_011538277.1:n.-57-823A>C
XM_017016437.1:c.-628A>C XP_016871926.1:n.-628A>C
XR_001747142.1:n.847A>C
XR_001747144.1:n.847A>C
XR_002956991.1:n.847A>C
XR_945788.2:n.847A>C
NM_021830.5:c.673A>C MANE Select NP_068602.2:p.Lys225Gln
NM_001163812.2:c.673A>C NP_001157284.1:p.Lys225Gln
NM_001163813.2:c.-119-761A>C NP_001157285.1:n.-119-761A>C
NM_001163814.2:c.-119-761A>C NP_001157286.1:n.-119-761A>C
NM_001368275.1:c.-57-823A>C NP_001355204.1:n.-57-823A>C
NR_160738.1:n.1341A>C
NR_160739.1:n.72-761A>C
NR_160740.1:n.1341A>C
NR_160741.1:n.1341A>C
NR_160742.1:n.1341A>C