Canonical Allele Identifier: CA291429
Gene: ZSWIM7 HGNC NCBI
TTC19 HGNC NCBI

Linked Data

ClinVar Variation Id: 137769
dbSNP Id: rs200004394

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.15999509G>C , CM000679.2:g.15999509G>C GRCh38
NC_000017.10:g.15902823G>C , CM000679.1:g.15902823G>C GRCh37
NC_000017.9:g.15843548G>C NCBI36
NG_029806.1:g.5130G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000399277.6:c.76+10C>G (ZSWIM7) MANE Select ENSP00000382218.1:n.76+10C>G
ENST00000261647.9:c.-340G>C (TTC19) ENSP00000261647.5:n.-340G>C
ENST00000399277.5:c.76+10C>G (ZSWIM7) ENSP00000382218.1:n.76+10C>G
ENST00000399280.6:n.35+151C>G (ZSWIM7)
ENST00000460252.5:c.86C>G (ZSWIM7) ENSP00000464463.1:p.Pro29Arg
ENST00000460315.5:c.86C>G (ZSWIM7) ENSP00000462590.1:p.Pro29Arg
ENST00000472495.5:c.76+10C>G (ZSWIM7) ENSP00000419138.1:n.76+10C>G
ENST00000474716.5:c.86C>G (ZSWIM7) ENSP00000464500.1:p.Pro29Arg
ENST00000476496.5:c.80C>G (ZSWIM7) ENSP00000462208.1:p.Pro27Arg
ENST00000486655.5:c.31+10C>G (ZSWIM7) ENSP00000464371.1:n.31+10C>G
ENST00000486706.6:c.86C>G (ZSWIM7) ENSP00000463327.1:p.Pro29Arg
ENST00000490395.5:c.86C>G (ZSWIM7) ENSP00000464605.1:p.Pro29Arg
ENST00000491631.5:c.86C>G (ZSWIM7) ENSP00000462598.1:p.Pro29Arg
ENST00000495825.6:n.24+151C>G (ZSWIM7)
ENST00000497719.5:n.54+151C>G (ZSWIM7)
ENST00000579955.1:c.86C>G (ZSWIM7) ENSP00000463444.1:p.Pro29Arg
ENST00000584519.5:c.76+10C>G (ZSWIM7) ENSP00000463592.1:n.76+10C>G
ENST00000585208.5:c.86C>G (ZSWIM7) ENSP00000464227.1:p.Pro29Arg
NM_001042697.1:c.76+10C>G (ZSWIM7) NP_001036162.1:n.76+10C>G
NM_001042698.1:c.76+10C>G (ZSWIM7) NP_001036163.1:n.76+10C>G
NM_001271420.1:c.-798G>C (TTC19) NP_001258349.1:n.-798G>C
NM_017775.3:c.-340G>C (TTC19) NP_060245.3:n.-340G>C
NM_001042697.2:c.76+10C>G (ZSWIM7) MANE Select NP_001036162.1:n.76+10C>G
NM_001042698.2:c.76+10C>G (ZSWIM7) NP_001036163.1:n.76+10C>G