Canonical Allele Identifier: CA984540748

Gene: CA10

Linked Data

• gnomAD v3: 17-51653012-TAAACAAA-T
• gnomAD v4: 17-51653012-TAAACAAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.51653013_51653019del , CM000679.2:g.51653013_51653019del	GRCh38
NC_000017.10:g.49730374_49730380del , CM000679.1:g.49730374_49730380del	GRCh37
NC_000017.9:g.47085373_47085379del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000451037.7:c.561+622_561+628del MANE Select	ENSP00000405388.2:n.561+622_561+628del
ENST00000285273.8:c.561+622_561+628del	ENSP00000285273.4:n.561+622_561+628del
ENST00000442502.6:c.561+622_561+628del	ENSP00000390666.2:n.561+622_561+628del
ENST00000451037.6:c.561+622_561+628del	ENSP00000405388.2:n.561+622_561+628del
ENST00000570565.5:c.336+622_336+628del	ENSP00000459619.1:n.336+622_336+628del
ENST00000571371.5:c.*603+622_*603+628del	ENSP00000461908.1:n.*603+622_*603+628del
ENST00000571918.1:n.400+622_400+628del
ENST00000575181.1:c.561+622_561+628del	ENSP00000460238.1:n.561+622_561+628del
NM_001082533.1:c.561+622_561+628del	NP_001076002.1:n.561+622_561+628del
NM_001082534.1:c.561+622_561+628del	NP_001076003.1:n.561+622_561+628del
NM_020178.4:c.561+622_561+628del	NP_064563.1:n.561+622_561+628del
XR_934507.1:n.401+622_401+628del
XM_017024878.2:c.270+622_270+628del	XP_016880367.1:n.270+622_270+628del
NM_020178.5:c.561+622_561+628del MANE Select	NP_064563.1:n.561+622_561+628del
NM_001082534.2:c.561+622_561+628del	NP_001076003.1:n.561+622_561+628del