Canonical Allele Identifier: CA1064142713

Gene: ALB

Linked Data

• dbSNP Id: rs1719108381
• gnomAD v3: 4-73420124-TA-T
• gnomAD v4: 4-73420124-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420127del , CM000666.2:g.73420127del	GRCh38
NC_000004.11:g.74285844del , CM000666.1:g.74285844del	GRCh37
NC_000004.10:g.74504708del	NCBI36
NG_009291.1:g.20873del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1786-127del MANE Select	ENSP00000295897.4:n.1786-127del
ENST00000295897.8:c.1786-127del	ENSP00000295897.4:n.1786-127del
ENST00000401494.7:c.1441-127del	ENSP00000384695.3:n.1441-127del
ENST00000415165.6:c.1210-127del	ENSP00000401820.2:n.1210-127del
ENST00000476441.6:c.*1065-127del	ENSP00000423727.1:n.*1065-127del
ENST00000495173.1:n.94-127del
ENST00000503124.5:c.1336-127del	ENSP00000421027.1:n.1336-127del
ENST00000505649.5:n.1333-127del
ENST00000508932.5:n.176-127del
ENST00000509063.5:c.1785+488del	ENSP00000422784.1:n.1785+488del
ENST00000511370.1:c.1319-127del
ENST00000621085.4:c.1147-127del	ENSP00000483421.1:n.1147-127del
ENST00000621628.4:c.1147-127del	ENSP00000480485.1:n.1147-127del
NM_000477.5:c.1786-127del	NP_000468.1:n.1786-127del
NM_000477.6:c.1786-127del	NP_000468.1:n.1786-127del
NM_000477.7:c.1786-127del MANE Select	NP_000468.1:n.1786-127del