Canonical Allele Identifier: CA1468148588

Gene: ALB

Linked Data

• dbSNP Id: rs1694941158

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419938_73419939insTTTTT , CM000666.2:g.73419938_73419939insTTTTT	GRCh38
NC_000004.11:g.74285655_74285656insTTTTT , CM000666.1:g.74285655_74285656insTTTTT	GRCh37
NC_000004.10:g.74504519_74504520insTTTTT	NCBI36
NG_009291.1:g.20684_20685insTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1785+299_1785+300insTTTTT MANE Select	ENSP00000295897.4:n.1785+299_1785+300insTTTTT
ENST00000295897.8:c.1785+299_1785+300insTTTTT	ENSP00000295897.4:n.1785+299_1785+300insTTTTT
ENST00000401494.7:c.1440+299_1440+300insTTTTT	ENSP00000384695.3:n.1440+299_1440+300insTTTTT
ENST00000415165.6:c.1209+299_1209+300insTTTTT	ENSP00000401820.2:n.1209+299_1209+300insTTTTT
ENST00000476441.6:c.*1064+299_*1064+300insTTTTT	ENSP00000423727.1:n.*1064+299_*1064+300insTTTTT
ENST00000495173.1:n.93+299_93+300insTTTTT
ENST00000503124.5:c.1335+299_1335+300insTTTTT	ENSP00000421027.1:n.1335+299_1335+300insTTTTT
ENST00000505649.5:n.1332+299_1332+300insTTTTT
ENST00000508932.5:n.176-316_176-315insTTTTT
ENST00000509063.5:c.1785+299_1785+300insTTTTT	ENSP00000422784.1:n.1785+299_1785+300insTTTTT
ENST00000511370.1:c.1318+299_1318+300insTTTTT
ENST00000621085.4:c.1146+299_1146+300insTTTTT	ENSP00000483421.1:n.1146+299_1146+300insTTTTT
ENST00000621628.4:c.1146+299_1146+300insTTTTT	ENSP00000480485.1:n.1146+299_1146+300insTTTTT
NM_000477.5:c.1785+299_1785+300insTTTTT	NP_000468.1:n.1785+299_1785+300insTTTTT
NM_000477.6:c.1785+299_1785+300insTTTTT	NP_000468.1:n.1785+299_1785+300insTTTTT
NM_000477.7:c.1785+299_1785+300insTTTTT MANE Select	NP_000468.1:n.1785+299_1785+300insTTTTT