Canonical Allele Identifier: CA2676143200
Gene: HAND1 HGNC NCBI

Linked Data

gnomAD v4: 5-154477399-CTGCATGGCCTGAGGCTGCTCACCGCTCCTGCACCCTTGGCTGGAGCA-C
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154477404_154477450del , CM000667.2:g.154477404_154477450del GRCh38
NC_000005.9:g.153856964_153857010del , CM000667.1:g.153856964_153857010del GRCh37
NC_000005.8:g.153837157_153837203del NCBI36
NG_052889.1:g.5819_5865del

Transcript Alleles

HGVS Amino-acid change
ENST00000231121.3:c.543+20_543+66del MANE Select ENSP00000231121.2:n.543+20_543+66del
ENST00000231121.2:c.543+20_543+66del ENSP00000231121.2:n.543+20_543+66del
NM_004821.2:c.543+20_543+66del NP_004812.1:n.543+20_543+66del
XM_005268531.1:c.543+20_543+66del XP_005268588.1:n.543+20_543+66del
NM_004821.3:c.543+20_543+66del MANE Select NP_004812.1:n.543+20_543+66del
Search 100 bp 5'
Search 100 bp 3'