Canonical Allele Identifier: CA1326925010

Gene: VWC2L

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214477166C= , CM000664.2:g.214477166C=	GRCh38
NC_000002.11:g.215341890C= , CM000664.1:g.215341890C=	GRCh37
NC_000002.10:g.215050135C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312504.10:c.520+40408C= MANE Select	ENSP00000308976.5:n.520+40408C=
ENST00000312504.9:c.520+40408C=	ENSP00000308976.5:n.520+40408C=
ENST00000427124.1:c.390+62583C=	ENSP00000403779.1:n.390+62583C=
NM_001080500.2:c.520+40408C=	NP_001073969.1:n.520+40408C=
XM_011511182.1:c.390+62583C=	XP_011509484.1:n.390+62583C=
NM_001080500.3:c.520+40408C=	NP_001073969.1:n.520+40408C=
NM_001345929.1:c.390+62583C=	NP_001332858.1:n.390+62583C=
NM_001080500.4:c.520+40408C= MANE Select	NP_001073969.1:n.520+40408C=
NM_001345929.2:c.390+62583C=	NP_001332858.1:n.390+62583C=
NR_159945.1:n.1333+40408C=