Canonical Allele Identifier: CA552305324
Gene: ALB HGNC NCBI

Linked Data

dbSNP Id: rs55764359

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73409167_73409172dup , CM000666.2:g.73409167_73409172dup GRCh38
NC_000004.11:g.74274884_74274889dup , CM000666.1:g.74274884_74274889dup GRCh37
NC_000004.10:g.74493748_74493753dup NCBI36
NG_009291.1:g.9913_9918dup

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.483-188_483-183dup MANE Select ENSP00000295897.4:n.483-188_483-183dup
ENST00000295897.8:c.483-188_483-183dup ENSP00000295897.4:n.483-188_483-183dup
ENST00000401494.7:c.138-188_138-183dup ENSP00000384695.3:n.138-188_138-183dup
ENST00000415165.6:c.138-2829_138-2824dup ENSP00000401820.2:n.138-2829_138-2824dup
ENST00000441319.5:c.489-188_489-183dup ENSP00000392541.1:n.489-188_489-183dup
ENST00000476441.6:c.80-188_80-183dup ENSP00000423727.1:n.80-188_80-183dup
ENST00000503124.5:c.33-188_33-183dup ENSP00000421027.1:n.33-188_33-183dup
ENST00000505649.5:n.169-188_169-183dup
ENST00000509063.5:c.483-188_483-183dup ENSP00000422784.1:n.483-188_483-183dup
ENST00000514786.1:n.452-188_452-183dup
ENST00000621085.4:c.483-188_483-183dup ENSP00000483421.1:n.483-188_483-183dup
ENST00000621628.4:c.486+91_486+96dup ENSP00000480485.1:n.486+91_486+96dup
NM_000477.5:c.483-188_483-183dup NP_000468.1:n.483-188_483-183dup
NM_000477.6:c.483-188_483-183dup NP_000468.1:n.483-188_483-183dup
NM_000477.7:c.483-188_483-183dup MANE Select NP_000468.1:n.483-188_483-183dup