Canonical Allele Identifier: CA552612221
Gene: UGT2B15 HGNC NCBI

Linked Data

gnomAD v2: 4-69512858-C-CTTTTTTT
MyVariant Identifiers: chr4:g.69512858_69512859insTTTTTTT (hg19) chr4:g.68647140_68647141insTTTTTTT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68647143_68647144insTTTTTTT , CM000666.2:g.68647143_68647144insTTTTTTT GRCh38
NC_000004.11:g.69512861_69512862insTTTTTTT , CM000666.1:g.69512861_69512862insTTTTTTT GRCh37
NC_000004.10:g.69195456_69195457insTTTTTTT NCBI36
NG_052676.1:g.28636_28637insAAAAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.1556_1557insAAAAAAA MANE Select ENSP00000341045.5:p.Leu520LysfsTer20
ENST00000338206.5:c.1556_1557insAAAAAAA ENSP00000341045.5:p.Leu520LysfsTer20
ENST00000616841.4:c.1556_1557insAAAAAAA ENSP00000482004.1:p.Leu520LysfsTer20
NM_001076.3:c.1556_1557insAAAAAAA NP_001067.2:p.Leu520LysfsTer20
NM_001076.4:c.1556_1557insAAAAAAA MANE Select NP_001067.2:p.Leu520LysfsTer20
Search 100 bp 5'
Search 100 bp 3'