Canonical Allele Identifier: CA1290830263

Gene: LCT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135806953_135806954delinsTG , CM000664.2:g.135806953_135806954delinsTG	GRCh38
NC_000002.11:g.136564523_136564524delinsTG , CM000664.1:g.136564523_136564524delinsTG	GRCh37
NC_000002.10:g.136280993_136280994delinsTG	NCBI36
NG_008104.2:g.53216_53217delinsCA , LRG_338:g.53216_53217delinsCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000264162.7:c.4173+174_4173+175delinsCA MANE Select	ENSP00000264162.2:n.4173+174_4173+175delinsCA
ENST00000264162.6:c.4173+174_4173+175delinsCA	ENSP00000264162.2:n.4173+174_4173+175delinsCA
ENST00000452974.1:c.2469+174_2469+175delinsCA	ENSP00000391231.1:n.2469+174_2469+175delinsCA
NM_002299.2:c.4173+174_4173+175delinsCA , LRG_338t1:c.4173+174_4173+175delinsCA	NP_002290.2:n.4173+174_4173+175delinsCA
NM_002299.3:c.4173+174_4173+175delinsCA	NP_002290.2:n.4173+174_4173+175delinsCA
XM_017004088.2:c.4173+174_4173+175delinsCA	XP_016859577.1:n.4173+174_4173+175delinsCA
NM_002299.4:c.4173+174_4173+175delinsCA MANE Select	NP_002290.2:n.4173+174_4173+175delinsCA