Canonical Allele Identifier: CA1184366831

Gene: SLC30A7 HNRNPA1P68

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.100941826C= , CM000663.2:g.100941826C=	GRCh38
NC_000001.10:g.101407382C= , CM000663.1:g.101407382C=	GRCh37
NC_000001.9:g.101179970C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357650.9:c.842+19985C= (SLC30A7) MANE Select	ENSP00000350278.4:n.842+19985C=
ENST00000357650.8:c.842+19985C= (SLC30A7)	ENSP00000350278.4:n.842+19985C=
ENST00000370112.8:c.842+19985C= (SLC30A7)	ENSP00000359130.4:n.842+19985C=
ENST00000425806.2:n.170G= (HNRNPA1P68)
NM_001144884.1:c.842+19985C= (SLC30A7)	NP_001138356.1:n.842+19985C=
NM_133496.4:c.842+19985C= (SLC30A7)	NP_598003.2:n.842+19985C=
XM_011540779.1:c.632+19985C= (SLC30A7)	XP_011539081.1:n.632+19985C=
XR_246237.2:n.1027+19985C= (SLC30A7)
XM_011540779.3:c.632+19985C= (SLC30A7)	XP_011539081.1:n.632+19985C=
XM_017000400.2:c.842+19985C= (SLC30A7)	XP_016855889.1:n.842+19985C=
XR_246237.3:n.1013+19985C= (SLC30A7)
NM_133496.5:c.842+19985C= (SLC30A7) MANE Select	NP_598003.2:n.842+19985C=
NM_001144884.2:c.842+19985C= (SLC30A7)	NP_001138356.1:n.842+19985C=