Canonical Allele Identifier: CA1064140860

Gene: ALB

Linked Data

• dbSNP Id: rs1718970050
• gnomAD v3: 4-73414651-CACCA-C
• gnomAD v4: 4-73414651-CACCA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73414652_73414655del , CM000666.2:g.73414652_73414655del	GRCh38
NC_000004.11:g.74280369_74280372del , CM000666.1:g.74280369_74280372del	GRCh37
NC_000004.10:g.74499233_74499236del	NCBI36
NG_009291.1:g.15398_15401del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1059-383_1059-380del MANE Select	ENSP00000295897.4:n.1059-383_1059-380del
ENST00000295897.8:c.1059-383_1059-380del	ENSP00000295897.4:n.1059-383_1059-380del
ENST00000401494.7:c.714-383_714-380del	ENSP00000384695.3:n.714-383_714-380del
ENST00000415165.6:c.483-383_483-380del	ENSP00000401820.2:n.483-383_483-380del
ENST00000476441.6:c.*338-383_*338-380del	ENSP00000423727.1:n.*338-383_*338-380del
ENST00000484992.1:n.379-383_379-380del
ENST00000503124.5:c.609-383_609-380del	ENSP00000421027.1:n.609-383_609-380del
ENST00000504043.1:n.62-383_62-380del
ENST00000505649.5:n.745-383_745-380del
ENST00000509063.5:c.1059-383_1059-380del	ENSP00000422784.1:n.1059-383_1059-380del
ENST00000511370.1:c.592-383_592-380del
ENST00000621085.4:c.491-454_491-451del	ENSP00000483421.1:n.491-454_491-451del
ENST00000621628.4:c.487-450_487-447del	ENSP00000480485.1:n.487-450_487-447del
NM_000477.5:c.1059-383_1059-380del	NP_000468.1:n.1059-383_1059-380del
NM_000477.6:c.1059-383_1059-380del	NP_000468.1:n.1059-383_1059-380del
NM_000477.7:c.1059-383_1059-380del MANE Select	NP_000468.1:n.1059-383_1059-380del