Canonical Allele Identifier: CA471157875

Gene: CWF19L1

Linked Data

• MyVariant Identifiers: chr10:g.102005584A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100245827A>C , CM000672.2:g.100245827A>C	GRCh38
NC_000010.10:g.102005584A>C , CM000672.1:g.102005584A>C	GRCh37
NC_000010.9:g.101995574A>C	NCBI36
NG_041811.1:g.26855T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354105.10:c.936T>G MANE Select	ENSP00000326411.6:p.Ser312=
ENST00000354105.8:c.936T>G	ENSP00000326411.6:p.Ser312=
ENST00000370379.1:c.201T>G	ENSP00000359405.1:p.Ser67=
ENST00000466408.1:n.290T>G
ENST00000466955.5:n.477T>G
ENST00000468709.5:n.792T>G
ENST00000478047.1:n.1199+7594T>G
ENST00000482452.5:n.624T>G
ENST00000496796.5:n.700T>G
NM_001303404.1:c.936T>G	NP_001290333.1:p.Ser312=
NM_001303405.1:c.525T>G	NP_001290334.1:p.Ser175=
NM_001303406.1:c.525T>G	NP_001290335.1:p.Ser175=
NM_001303407.1:c.201T>G	NP_001290336.1:p.Ser67=
NM_018294.5:c.936T>G	NP_060764.3:p.Ser312=
NM_018294.6:c.936T>G MANE Select	NP_060764.3:p.Ser312=
NM_001303404.2:c.936T>G	NP_001290333.1:p.Ser312=
NM_001303405.2:c.525T>G	NP_001290334.1:p.Ser175=
NM_001303406.2:c.525T>G	NP_001290335.1:p.Ser175=
NM_001303407.2:c.201T>G	NP_001290336.1:p.Ser67=