Canonical Allele Identifier: CA2631192656
Gene: ABCA3 HGNC NCBI
ABCA17P HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2340497_2340499del , CM000678.2:g.2340497_2340499del GRCh38
NC_000016.9:g.2390498_2390500del , CM000678.1:g.2390498_2390500del GRCh37
NC_000016.8:g.2330499_2330501del NCBI36
NG_011790.1:g.5250_5252del

Transcript Alleles

HGVS Amino-acid change
ENST00000301732.10:c.-539+76_-539+78del (ABCA3) MANE Select ENSP00000301732.5:n.-539+76_-539+78del
ENST00000640929.1:n.42+1166_42+1168del (ABCA17P)
ENST00000301732.9:c.-539+76_-539+78del (ABCA3) ENSP00000301732.5:n.-539+76_-539+78del
ENST00000382381.7:c.-539+76_-539+78del (ABCA3) ENSP00000371818.3:n.-539+76_-539+78del
ENST00000512848.5:n.182+1166_182+1168del (ABCA17P)
ENST00000563623.5:n.25+76_25+78del (ABCA3)
NM_001089.2:c.-539+76_-539+78del (ABCA3) NP_001080.2:n.-539+76_-539+78del
NM_001089.3:c.-539+76_-539+78del (ABCA3) MANE Select NP_001080.2:n.-539+76_-539+78del