Canonical Allele Identifier: CA2277119

Linked Data

dbSNP Id: rs749765035
gnomAD v2: 3-15643067-C-T
gnomAD v4: 3-15601560-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.15601560C>T , CM000665.2:g.15601560C>T GRCh38
NC_000003.11:g.15643067C>T , CM000665.1:g.15643067C>T GRCh37
NC_000003.10:g.15618071C>T NCBI36
NG_008019.1:g.4813C>T
NG_008019.2:g.5209C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000321169.10:c.-97G>A (HACL1) MANE Select ENSP00000323811.5:n.-97G>A
ENST00000427382.2:c.-104C>T (BTD) ENSP00000397113.2:n.-104C>T
ENST00000449107.7:c.-227C>T (BTD) ENSP00000388212.2:n.-227C>T
ENST00000321169.9:c.-97G>A (HACL1) ENSP00000323811.5:n.-97G>A
ENST00000414979.1:c.-97G>A (HACL1) ENSP00000395352.1:n.-97G>A
ENST00000417015.1:c.156C>T (BTD) ENSP00000403775.1:p.Tyr52=
ENST00000421993.5:c.-97G>A (HACL1) ENSP00000391393.1:n.-97G>A
ENST00000422591.5:c.-97G>A (HACL1) ENSP00000392796.1:n.-97G>A
ENST00000427382.1:c.-104C>T (BTD) ENSP00000397113.1:n.-104C>T
ENST00000435217.6:c.-97G>A (HACL1) ENSP00000395278.2:n.-97G>A
ENST00000451445.6:c.-97G>A (HACL1) ENSP00000403656.2:n.-97G>A
ENST00000456194.6:c.-97G>A (HACL1) ENSP00000390699.2:n.-97G>A
ENST00000457447.6:c.-97G>A (HACL1) ENSP00000404883.2:n.-97G>A
ENST00000460907.1:n.10G>A (HACL1)
ENST00000494021.1:n.191C>T (BTD)
ENST00000628377.2:c.-97G>A (HACL1) ENSP00000486684.1:n.-97G>A
NM_001281723.1:c.-161C>T (BTD) NP_001268652.1:n.-161C>T
NM_001284413.1:c.-97G>A (HACL1) NP_001271342.1:n.-97G>A
NM_001284415.1:c.-97G>A (HACL1) NP_001271344.1:n.-97G>A
NM_001284416.1:c.-97G>A (HACL1) NP_001271345.1:n.-97G>A
NM_012260.3:c.-97G>A (HACL1) NP_036392.2:n.-97G>A
NR_104315.1:n.293G>A (HACL1)
NM_001281723.2:c.-161C>T (BTD) NP_001268652.1:n.-161C>T
NM_001281723.3:c.-227C>T (BTD) NP_001268652.2:n.-227C>T
NM_001284413.2:c.-97G>A (HACL1) NP_001271342.1:n.-97G>A
NM_001284415.2:c.-97G>A (HACL1) NP_001271344.1:n.-97G>A
NM_001284416.2:c.-97G>A (HACL1) NP_001271345.1:n.-97G>A
NM_012260.4:c.-97G>A (HACL1) MANE Select NP_036392.2:n.-97G>A
NR_104315.2:n.10G>A (HACL1)