Canonical Allele Identifier: CA2670937205
Gene: ALB HGNC NCBI

Linked Data

dbSNP Id: rs2149327579

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73409172_73409173insAAAC , CM000666.2:g.73409172_73409173insAAAC GRCh38
NC_000004.11:g.74274889_74274890insAAAC , CM000666.1:g.74274889_74274890insAAAC GRCh37
NC_000004.10:g.74493753_74493754insAAAC NCBI36
NG_009291.1:g.9918_9919insAAAC

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.483-183_483-182insAAAC MANE Select ENSP00000295897.4:n.483-183_483-182insAAAC
ENST00000295897.8:c.483-183_483-182insAAAC ENSP00000295897.4:n.483-183_483-182insAAAC
ENST00000401494.7:c.138-183_138-182insAAAC ENSP00000384695.3:n.138-183_138-182insAAAC
ENST00000415165.6:c.138-2824_138-2823insAAAC ENSP00000401820.2:n.138-2824_138-2823insAAAC
ENST00000441319.5:c.489-183_489-182insAAAC ENSP00000392541.1:n.489-183_489-182insAAAC
ENST00000476441.6:c.80-183_80-182insAAAC ENSP00000423727.1:n.80-183_80-182insAAAC
ENST00000503124.5:c.33-183_33-182insAAAC ENSP00000421027.1:n.33-183_33-182insAAAC
ENST00000505649.5:n.169-183_169-182insAAAC
ENST00000509063.5:c.483-183_483-182insAAAC ENSP00000422784.1:n.483-183_483-182insAAAC
ENST00000514786.1:n.452-183_452-182insAAAC
ENST00000621085.4:c.483-183_483-182insAAAC ENSP00000483421.1:n.483-183_483-182insAAAC
ENST00000621628.4:c.486+96_486+97insAAAC ENSP00000480485.1:n.486+96_486+97insAAAC
NM_000477.5:c.483-183_483-182insAAAC NP_000468.1:n.483-183_483-182insAAAC
NM_000477.6:c.483-183_483-182insAAAC NP_000468.1:n.483-183_483-182insAAAC
NM_000477.7:c.483-183_483-182insAAAC MANE Select NP_000468.1:n.483-183_483-182insAAAC