Canonical Allele Identifier: CA367015486
Gene: TWIST1 HGNC NCBI

Linked Data

ClinVar Variation Id: 935674
ClinVar RCV Id: RCV001204316
dbSNP Id: rs1788580776
MyVariant Identifiers: chr7:g.19156529G>A (hg19) chr7:g.19116906G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.19116906G>A , CM000669.2:g.19116906G>A GRCh38
NC_000007.13:g.19156529G>A , CM000669.1:g.19156529G>A GRCh37
NC_000007.12:g.19123054G>A NCBI36
NG_008114.1:g.5767C>T
NG_008114.2:g.5767C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000242261.6:c.416C>T MANE Select ENSP00000242261.5:p.Pro139Leu
ENST00000242261.5:c.416C>T ENSP00000242261.5:p.Pro139Leu
ENST00000354571.5:c.213C>T
ENST00000443687.5:c.19C>T
NM_000474.3:c.416C>T NP_000465.1:p.Pro139Leu
XM_011515496.1:c.416C>T XP_011513798.1:p.Pro139Leu
NR_149001.1:n.767C>T
NM_000474.4:c.416C>T MANE Select NP_000465.1:p.Pro139Leu
NR_149001.2:n.731C>T
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