Canonical Allele Identifier: CA2202146488
Gene: ABCA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2278777C= , CM000678.2:g.2278777C= GRCh38
NC_000016.9:g.2328778C= , CM000678.1:g.2328778C= GRCh37
NC_000016.8:g.2268779C= NCBI36
NG_011790.1:g.66970G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301732.10:c.4547+166G= MANE Select ENSP00000301732.5:n.4547+166G=
ENST00000301732.9:c.4547+166G= ENSP00000301732.5:n.4547+166G=
ENST00000382381.7:c.4373+166G= ENSP00000371818.3:n.4373+166G=
ENST00000566200.1:n.1068+166G=
NM_001089.2:c.4547+166G= NP_001080.2:n.4547+166G=
NM_001089.3:c.4547+166G= MANE Select NP_001080.2:n.4547+166G=