Canonical Allele Identifier: CA798286894

Gene: ALB

Linked Data

• dbSNP Id: rs1414223419
• gnomAD v3: 4-73409172-CTT-C
• gnomAD v4: 4-73409172-CTT-C
• MyVariant Identifiers: chr4:g.74274890_74274891del (hg19) ; chr4:g.73409173_73409174del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409173_73409174del , CM000666.2:g.73409173_73409174del	GRCh38
NC_000004.11:g.74274890_74274891del , CM000666.1:g.74274890_74274891del	GRCh37
NC_000004.10:g.74493754_74493755del	NCBI36
NG_009291.1:g.9919_9920del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.483-182_483-181del MANE Select	ENSP00000295897.4:n.483-182_483-181del
ENST00000295897.8:c.483-182_483-181del	ENSP00000295897.4:n.483-182_483-181del
ENST00000401494.7:c.138-182_138-181del	ENSP00000384695.3:n.138-182_138-181del
ENST00000415165.6:c.138-2823_138-2822del	ENSP00000401820.2:n.138-2823_138-2822del
ENST00000441319.5:c.489-182_489-181del	ENSP00000392541.1:n.489-182_489-181del
ENST00000476441.6:c.80-182_80-181del	ENSP00000423727.1:n.80-182_80-181del
ENST00000503124.5:c.33-182_33-181del	ENSP00000421027.1:n.33-182_33-181del
ENST00000505649.5:n.169-182_169-181del
ENST00000509063.5:c.483-182_483-181del	ENSP00000422784.1:n.483-182_483-181del
ENST00000514786.1:n.452-182_452-181del
ENST00000621085.4:c.483-182_483-181del	ENSP00000483421.1:n.483-182_483-181del
ENST00000621628.4:c.486+97_486+98del	ENSP00000480485.1:n.486+97_486+98del
NM_000477.5:c.483-182_483-181del	NP_000468.1:n.483-182_483-181del
NM_000477.6:c.483-182_483-181del	NP_000468.1:n.483-182_483-181del
NM_000477.7:c.483-182_483-181del MANE Select	NP_000468.1:n.483-182_483-181del