Canonical Allele Identifier: CA1290827578
Gene: LCT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135800566A= , CM000664.2:g.135800566A= GRCh38
NC_000002.11:g.136558136A= , CM000664.1:g.136558136A= GRCh37
NC_000002.10:g.136274606A= NCBI36
NG_008104.2:g.59604T= , LRG_338:g.59604T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264162.7:c.4866+41T= MANE Select ENSP00000264162.2:n.4866+41T=
ENST00000264162.6:c.4866+41T= ENSP00000264162.2:n.4866+41T=
ENST00000452974.1:c.2960-2428T= ENSP00000391231.1:n.2960-2428T=
NM_002299.2:c.4866+41T= , LRG_338t1:c.4866+41T= NP_002290.2:n.4866+41T=
NM_002299.3:c.4866+41T= NP_002290.2:n.4866+41T=
XM_017004088.2:c.4866+41T= XP_016859577.1:n.4866+41T=
NM_002299.4:c.4866+41T= MANE Select NP_002290.2:n.4866+41T=
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