Canonical Allele Identifier: CA552306228

Gene: ALB

Linked Data

• dbSNP Id: rs1247341023
• gnomAD v2: 4-74280502-GAGA-G
• gnomAD v3: 4-73414785-GAGA-G
• gnomAD v4: 4-73414785-GAGA-G
• MyVariant Identifiers: chr4:g.74280503_74280505del (hg19) ; chr4:g.73414786_73414788del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73414788_73414790del , CM000666.2:g.73414788_73414790del	GRCh38
NC_000004.11:g.74280505_74280507del , CM000666.1:g.74280505_74280507del	GRCh37
NC_000004.10:g.74499369_74499371del	NCBI36
NG_009291.1:g.15534_15536del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1059-247_1059-245del MANE Select	ENSP00000295897.4:n.1059-247_1059-245del
ENST00000295897.8:c.1059-247_1059-245del	ENSP00000295897.4:n.1059-247_1059-245del
ENST00000401494.7:c.714-247_714-245del	ENSP00000384695.3:n.714-247_714-245del
ENST00000415165.6:c.483-247_483-245del	ENSP00000401820.2:n.483-247_483-245del
ENST00000476441.6:c.*338-247_*338-245del	ENSP00000423727.1:n.*338-247_*338-245del
ENST00000484992.1:n.379-247_379-245del
ENST00000503124.5:c.609-247_609-245del	ENSP00000421027.1:n.609-247_609-245del
ENST00000504043.1:n.62-247_62-245del
ENST00000505649.5:n.745-247_745-245del
ENST00000509063.5:c.1059-247_1059-245del	ENSP00000422784.1:n.1059-247_1059-245del
ENST00000511370.1:c.592-247_592-245del
ENST00000621085.4:c.491-318_491-316del	ENSP00000483421.1:n.491-318_491-316del
ENST00000621628.4:c.487-314_487-312del	ENSP00000480485.1:n.487-314_487-312del
NM_000477.5:c.1059-247_1059-245del	NP_000468.1:n.1059-247_1059-245del
NM_000477.6:c.1059-247_1059-245del	NP_000468.1:n.1059-247_1059-245del
NM_000477.7:c.1059-247_1059-245del MANE Select	NP_000468.1:n.1059-247_1059-245del