Canonical Allele Identifier: CA2646785383

Gene: SLC30A7 HNRNPA1P68

Linked Data

• gnomAD v4: 1-100941670-CTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.100941671_100941672del , CM000663.2:g.100941671_100941672del	GRCh38
NC_000001.10:g.101407227_101407228del , CM000663.1:g.101407227_101407228del	GRCh37
NC_000001.9:g.101179815_101179816del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357650.9:c.842+19830_842+19831del (SLC30A7) MANE Select	ENSP00000350278.4:n.842+19830_842+19831del
ENST00000357650.8:c.842+19830_842+19831del (SLC30A7)	ENSP00000350278.4:n.842+19830_842+19831del
ENST00000370112.8:c.842+19830_842+19831del (SLC30A7)	ENSP00000359130.4:n.842+19830_842+19831del
ENST00000425806.2:n.324_325del (HNRNPA1P68)
NM_001144884.1:c.842+19830_842+19831del (SLC30A7)	NP_001138356.1:n.842+19830_842+19831del
NM_133496.4:c.842+19830_842+19831del (SLC30A7)	NP_598003.2:n.842+19830_842+19831del
XM_011540779.1:c.632+19830_632+19831del (SLC30A7)	XP_011539081.1:n.632+19830_632+19831del
XR_246237.2:n.1027+19830_1027+19831del (SLC30A7)
XM_011540779.3:c.632+19830_632+19831del (SLC30A7)	XP_011539081.1:n.632+19830_632+19831del
XM_017000400.2:c.842+19830_842+19831del (SLC30A7)	XP_016855889.1:n.842+19830_842+19831del
XR_246237.3:n.1013+19830_1013+19831del (SLC30A7)
NM_133496.5:c.842+19830_842+19831del (SLC30A7) MANE Select	NP_598003.2:n.842+19830_842+19831del
NM_001144884.2:c.842+19830_842+19831del (SLC30A7)	NP_001138356.1:n.842+19830_842+19831del